Made in India new generation heart stent receives major global recognition

An Indian-made heart stent, Supraflex Cruz, has demonstrated a lower failure rate in high-risk patients compared to a US-made market leader. The TUXEDO-2 trial, conducted in India, showed the Indian stent to be non-inferior and resulted in significantly lower Target Lesion Failures, including cardiac death and heart attacks.

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Cipla plans 4 major respiratory launches by 2026 after beating Q2 estimates with highest-ever quarterly revenue of Rs 7,500+ cr

Cipla Ltd reported a record second-quarter revenue exceeding Rs 7,500 crore, driven by strong demand for its respiratory drugs and a growing chronic portfolio. The company maintained its second position in India's chronic market and saw significant progress in its U.S. respiratory and biosimilar segments, with four major respiratory assets slated for launch by 2026.

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Zero GST on health insurance plans sparks 38% surge in demand: Report

Health insurance demand has surged by 38 percent following the removal of GST. Individuals are now opting for higher coverage amounts, with the average sum insured increasing significantly. This trend is observed across various age groups and even in smaller cities. The exemption makes health and life insurance more affordable, encouraging comprehensive protection against rising healthcare costs.

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Drug cos forging data for approval, mislabelling brands to be barred

In a bold move to combat deception in the pharmaceutical industry, the government is instituting strict penalties for drugmakers caught submitting forged or misleading documents during the approval process. This initiative is a direct response to the tragic incidents of child fatalities linked to tainted cough syrups.

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Govt aligns packaging rules for medical devices, eases compliance burden

Attention healthcare providers: New packaging regulations for medical devices have just come into effect! These amendments are designed to ensure that packaging aligns seamlessly with existing medical device standards. This simplification not only supports businesses by streamlining compliance but also enhances clarity for consumers making informed choices.

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Amway to invest $12 million in India to enhance physical presence

Amway plans a USD 12 million investment in India over the next three to five years. This will establish new stores nationwide, aiming to boost Amway's presence. The company also intends to increase exports from India. Amway sees India as a significant growth market with strong potential for its health and wellness products.

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Indian pharma & healthcare sector saw $3.5 bn deals in Q3 2025: Grant Thornton Bharat

The Indian pharmaceutical and healthcare sector saw robust deal activity in Q3, with 72 transactions totaling USD 3.5 billion. This surge, driven by a sharp rebound in private deals and high-value acquisitions like Torrent Pharma's stake in JB Chemicals, reflects renewed investor confidence in the sector's growth potential and consolidation plays.

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Sanofi India appoints Deepak Arora as Managing Director

Sanofi India has appointed Deepak Arora as its new Managing Director. Arora will lead the company's strategic vision for India, aligning it with Sanofi's global strategy. He will focus on accelerating innovation and agility across the organization. Arora brings over 30 years of pharmaceutical and healthcare experience from various international markets. His appointment aims to enhance patient service throughout India.

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Dr Reddy’s gets nod to make generic semaglutide for weight loss

Dr Reddy's Laboratories is set to launch generic semaglutide, a popular weight loss drug. An expert committee has approved their proposal. The company plans to market the drug as soon as Novo Nordisk's patent expires early next year. This move aims to tap into a growing market for obesity and diabetes management. Dr Reddy's is preparing for a competitive launch.

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Lupin launches generic drug to treat urea cycle disorders in US

Drug firm Lupin has launched a generic medication in the US. This new drug treats urea cycle disorders. It is an authorized generic version of Ravicti oral liquid. The medication helps patients manage the disorder. This is for those who cannot be managed by diet alone. Lupin's shares saw a slight dip on the BSE.

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Time has never been better for Pharma breakthroughs than today: Bayer executive Stefan Oelrich

Bayer, the renowned pharmaceutical powerhouse from Germany, is implementing a tiered pricing strategy on a global scale to make medications more accessible. The CEO emphasizes the necessity of earning returns to justify research investments. As innovation ecosystems shift, particularly towards regions like China, Bayer is proactively adapting.

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Eli Lilly allows Cipla to sell weight loss drug under new brand in India

Eli Lilly and Cipla have joined forces. Cipla will now market Lilly's popular weight-loss drug in India. The medication will be sold under the brand name Yurpeak. This drug helps manage diabetes and obesity. It is administered as a once-weekly injection. Yurpeak will be available in multiple dose strengths.

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Biocon gets Health Canada nod for biosimilars Yesintek, Yesintek IV

Biocon Biologics has made strides in the healthcare sector by obtaining Health Canada’s approval for Yesintek and Yesintek IV, its latest autoimmune treatment options. These biosimilars to Stelara have received official clearance on October 17, heralding a new era of affordable treatment in Canada.

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Trump eyes fresh tariff probe focused on foreign drug prices

President Trump is initiating a new investigation into drug prices, aiming to compel foreign nations to pay the same as Americans for their medicines. This probe, under Section 301 of the Trade Act, could lead to tariffs or other trade actions against countries with lower drug costs, potentially escalating global trade tensions.

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Regulator to digitally monitor supply chain of cough syrups

In a groundbreaking effort to enhance public health safety, India's drug regulatory authority has unveiled a digital tracking system for cough syrup supplies. This initiative comes in response to alarming cases of harmful cough syrups surfacing in the market. The revamped Online National Drugs Licensing System now requires pharmaceutical manufacturers of solvents to register and obtain licenses through this portal.

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COVID-19 vaccines may help some cancer patients fight tumors

New research suggests COVID-19 mRNA vaccines could help cancer patients. Those with advanced lung or skin cancer who received Pfizer or Moderna shots lived longer while on immunotherapy. The mRNA technology appears to enhance the immune system's ability to fight tumors. This finding offers a potential new approach for cancer treatment, with further studies planned.

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CCI clears Torrent Pharma's proposal to buy stake in JB Chemicals

India's competition regulator CCI has approved Torrent Pharmaceuticals' acquisition of a stake in JB Chemicals and Pharmaceuticals. This deal, valued at Rs 19,500 crore, will make Torrent Pharmaceuticals the second most valued pharma company in India. The approval comes with voluntary modifications offered by both companies. This significant development marks a major consolidation in the Indian pharmaceutical sector.

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Dr Reddy's Srikakulam unit classified as voluntary action indicated by USFDA

Dr Reddy's Laboratories has received a report from the US Food and Drug Administration. The report concerns its manufacturing facility in Srikakulam, Andhra Pradesh. The USFDA has classified the inspection outcome as Voluntary Action Indicated. This means the inspection is officially closed. The company received the Establishment Inspection Report on October 20, 2025.

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Glenmark, Dr Reddy's recall products in US: USFDA

Indian drugmakers Glenmark and Dr Reddy's Laboratories are recalling products in the United States. Glenmark is recalling oral contraceptive medication due to failed impurities. Dr Reddy's Laboratories is recalling muscle relaxant medication due to out-of-specification results. These recalls are initiated by the US Food and Drug Administration. India has many USFDA-compliant plants outside the US.

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India develops first indigenously discovered antibiotic "Nafithromycin" effective against resistant respiratory infections

India has proudly introduced Nafithromycin, its first homegrown antibiotic, tackling stubborn respiratory infections with groundbreaking efficacy. Coupled with a significant leap in gene therapy for Haemophilia, these innovations underscore India's commitment to self-sufficiency in the pharmaceutical arena. The country is now embracing a model that fosters collaboration with the private sector, setting the stage for international acclaim in biomedical research.

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Strides Founder raises Rs 1000 crore to refinance debt

Arun Kumar, founder of Strides Group and OneSource, has secured ₹1,000 crore by pledging shares. This move refinances existing loans, extending maturities and simplifying repayments. The transaction aims to consolidate smaller borrowings into larger, long-term facilities. It reflects a broader effort to clean up the promoter's balance sheet and shows a decline in pledged shares, indicating deleveraging.

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Prerna launches CANTEL™: A MicroRNA-based blood test for breast cancer screening

PrecisionRNA Biotech from Hyderabad has launched Cantel, a new microRNA blood test for breast cancer screening. This test offers a simple and accurate alternative to traditional methods. It aims to improve early detection rates in India. Cantel is designed for women aged 30 and above. The company is seeking investors for nationwide expansion.

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Indian firms explore localisation of pharma production in Russia

The Russian market is attracting growing interest from Indian pharmaceutical companies exploring opportunities to establish production facilities across various regions of the country. This was announced by Moscow Government Minister and Head of the Department for External Economic and International Relations, Sergey Cheremin, during the " Russia-India. Mutual Efficiency" forum.

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US Senator raises alarm over poor-quality drug imports from India and China, seeks tougher FDA inspections

In a letter to FDA Commissioner Martin Makary, Banks said the agency must "do more to protect the US drug supply," warning that lax oversight could endanger American consumers. He pointed out that inspections of foreign drug plants have not yet returned to pre-pandemic levels, even as the number of manufacturers continues to grow.

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India to force drugmakers to upgrade plants after fatal cough syrup crisis

India has denied drugmakers more time to upgrade manufacturing facilities. This decision follows the deaths of at least 24 children from contaminated cough syrup. The government mandated World Health Organization standards after similar incidents abroad. Despite pleas from smaller firms, officials are firm on the deadline.

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Alchem International moves Delhi HC against single-judge order on ‘Alchem’ trademark

Alchem International is challenging a court order that stops it from using its name. The order prevents Alchem from selling products with the name 'Alchem' due to similarity with Alkem Laboratories' trademark. A division bench is reviewing the case. The court previously found the names phonetically identical. Alkem has used its trademark since 1973. Alchem started using its mark later.

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Heart blockages, tumors, fractures: Now, you can see what’s wrong inside your body in 3D at this Delhi govt hospital

Delhi-NCR's Vardhman Mahavir Medical College and Safdarjung Hospital has introduced a virtual clinical anatomy laboratory. Patients can now view detailed 3D models of their own bodies. This technology uses CT or MRI scans to create interactive visuals of organs, bones, and tissues. It helps patients understand their medical conditions and treatments better.

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Lords Mark Industries Ltd. secures US FDA Registration, reinforces India’s position in global healthcare manufacturing

Lords Mark Industries Ltd. has achieved a significant milestone with US FDA registration for its surgical consumables, orthopedic supports, and hygiene products. This recognition underscores the company's manufacturing excellence. It opens doors to international markets, boosting exports and India's global healthcare manufacturing standing. The approved portfolio covers a wide range of essential healthcare items.

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Under the scanner, yet generic cough syrups hit shelves

Worry spreads regarding the multitude of cough syrup brands circulating in India, with alarming revelations of toxic diethylene glycol detected in some, resulting in heartbreaking instances of child mortality. This situation sheds light on the questionable efficacy of regulatory measures, as many small-scale producers evade scrutiny.

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Centre plans new law for stricter quality checks and surveillance of drugs, medical devices, and cosmetics

India is creating a new law to improve drug quality and safety. This legislation will give more power to regulators for checking medicines, medical devices, and cosmetics. The aim is to prevent fake and substandard products. This move follows global concerns and recent incidents.

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Centre to bring law for strict quality checks, surveillance of drugs and cosmetics

India is creating a new law to improve drug quality and safety. This legislation will give more power to regulators for testing and monitoring medicines, medical devices, and cosmetics. The aim is to ensure stricter compliance and accountability. This move follows global concerns and recent incidents.

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Cloudnine Hospitals leads race to acquire Apollo Cradle

Cloudnine Hospitals is stepping into a pivotal role in the maternity and pediatric care sphere, as it engages in advanced discussions to acquire Apollo Cradle and Children's Hospital at a valuation of around ₹1,500 crore. Having signed an exclusivity pact, Cloudnine has kicked off due diligence procedures.

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Roche moves SC against Natco’s launch of generic Risdiplam in India

F. Hoffmann-La Roche AG has approached the Supreme Court. This follows a Delhi High Court decision permitting Natco Pharma to introduce a generic version of Risdiplam. Risdiplam treats spinal muscular atrophy. The High Court rejected Roche's plea to halt Natco's manufacturing. Natco plans to sell the drug at a significantly lower price.

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India accuses Balaji Amines of making pharma-grade chemical without a drug-making licence

Balaji Amines faces accusations from Indian authorities for producing pharma-grade propylene glycol without a necessary drug manufacturing license. This comes after some batches were found to be substandard. The company states it only manufactured technical and food-grade PG for non-pharma clients. Investigations are ongoing, and the company's stock has seen a decline.

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Aurobindo Pharma promoters raise Rs 2k cr to fund realty, other asset buys

The transaction is split into two parts. The Rs 650 crore Series 1 comes with a 24-month tenor and a two-year put and call option, and Rs 1,450 crore, which will be Series 2 with a four-year tenor. Series 1 will carry a coupon of 11.75%, while Series 2 is likely to be priced at 15.5%.

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WHO warns of contaminated India cough syrups linked to 17 child deaths

The World Health Organization has issued a health advisory regarding three contaminated cough syrups from India. Specific batches of COLDRIF, Respifresh TR, and ReLife are identified. These products pose severe health risks. India's Central Drugs Standard Control Organization reported that 17 children under five died after consuming these syrups. Authorities confirm no contaminated medicines were exported from India.

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Cough Syrup deaths: Sresan Pharmaceuticals' license cancelled, company shut down

Tamil Nadu has cancelled the manufacturing license of Sresan Pharmaceutical, maker of Coldrif cough syrup, after it was linked to at least 22 deaths in Madhya Pradesh due to toxic contaminants. The state ordered comprehensive inspections of all pharmaceutical units following the incident and the arrest of the company owner.

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ED raids seven Chennai sites linked to Sreesan Pharma over Coldrif cough syrup deaths

The Enforcement Directorate (ED) conducted searches at seven locations in Chennai concerning the Coldrif cough syrup case. These raids, under the PMLA, are linked to Sreesan Pharma, the manufacturer of the banned syrup. The cough syrup has been linked to the deaths of approximately 22 children, primarily in Madhya Pradesh and Rajasthan.

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DRL, Zydus recall drugs in US over manufacturing issues: USFDA

Dr Reddy's Laboratories and Zydus Lifesciences are recalling products in the US due to manufacturing issues. Dr Reddy's is recalling muscle relaxant injections over stability testing failures, while Zydus Lifesciences is recalling antiviral medication for failing impurity specifications. Both recalls are classified as Class II by the USFDA.

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Survey finds 90% Indians willing to pay more for certified healthcare

A Ficci and EY-Parthenon report reveals that 83% of Indian patients desire accessible healthcare information, with nearly 90% willing to pay more for certified quality. Despite India's healthcare efficiency, a national framework for clear quality standards is needed to empower informed patient choices.

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Breast cancer cases on rise; junk food, lack of exercise contributing factors: Doctors

Breast cancer is a growing concern in India, projected to reach two lakh cases annually by 2030. Experts highlight lifestyle factors like lack of exercise, obesity, and westernized diets as key contributors. Genetic predispositions also play a role, necessitating increased genetic testing and early screening for high-risk individuals.

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Natco Pharma to acquire significant stake in S African firm Adcock Ingram

Indian pharmaceutical company Natco Pharma is set to acquire significant stakes in South Africa's Adcock Ingram, a 135-year-old firm, in a R4.2 billion deal. This acquisition will make Adcock Ingram a privately-held entity, co-owned by Natco and Bidvest, with Adcock Ingram delisting from the JSE post-completion.

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Max Healthcare plans over ₹5,000 crore expansion, eyes pan-India presence: MD Abhay Soi

Max Healthcare has surpassed ₹1 lakh crore in market capitalization, becoming India's most valued healthcare company. The company plans a significant capex of over ₹5,000 crore for expansion, aiming to increase bed capacity substantially and extend its reach into tier-2 and tier-3 cities across India.

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Panacea Biotec bags Rs 127 crore order for oral polio vaccines

Panacea Biotec has secured a significant deal to supply bivalent oral polio vaccines valued at Rs 127.2 crore to the Central Medical Services Society. This crucial supply, confirmed via a Letter of Acceptance, will be delivered in multiple phases over 90 to 480 days, bolstering India's ongoing polio eradication efforts.

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Trump & Co said to have shelved generic drug tariffs, Indian pharma stocks get booster dose

The Trump White House has halted plans for tariffs on generic drug imports, a decision welcomed by Indian pharmaceutical companies that supply nearly half of US generic prescriptions. This move reassures millions of Americans relying on affordable imported medications for various health conditions, averting potential price hikes and shortages.

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MP cough syrup deaths: Maharashtra FDA orders inspection of liquid oral formulations

Following the deaths of 20 children in Madhya Pradesh due to a contaminated cough syrup, the Maharashtra FDA has initiated a special drive. This includes inspecting manufacturers and testing liquid oral formulations from hospitals and distributors to ensure quality and prevent similar incidents.

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Drug regulatory body steps up heat on state units amid cough syrup lapses

India's drug regulator has directed state authorities to enforce strict testing of all raw materials used in medicines. This action follows the tragic deaths of children due to contaminated cough syrups. Investigations revealed manufacturers were not testing excipients, leading to the use of industrial-grade materials unfit for human consumption.

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Eli Lilly's obesity drug Mounjaro's India sales hit a sweet spot within six months of launch

Lilly's Mounjaro has rapidly become the second-highest selling drug in India's pharmaceutical market, achieving ₹233 crore in sales within six months of its March launch. The weight-loss and diabetes medication posted ₹80 crore in September sales, surpassing popular brands and attributed to its superior efficacy and first-mover advantage over competitors.

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Sresan Pharma, maker of Coldrif, broke multiple rules: Officials

Sresan Pharma, the manufacturer of Coldrif cough syrup linked to at least 16 child deaths, allegedly ignored numerous quality standards. A central inspection revealed a "shoddy and neglected state" at their Tamil Nadu facility, with significant violations in raw material testing and batch release.

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The first 90 days: A doctor’s checklist for people newly diagnosed with type 2 diabetes

The first 90 days after a type 2 diabetes diagnosis are crucial for managing the condition and reducing heart disease risks. Experts emphasize understanding the body's response to high blood sugar, adopting healthy lifestyle foundations like smart eating and regular exercise, and seeking support to lay the groundwork for long-term health.

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Eli Lilly to invest $1 billion in India, expand manufacturing and introduce oral weight-loss drug

Eli Lilly is significantly expanding its Indian operations with over $1 billion in contract manufacturing investments and plans for a global capability center. The US pharma giant is positioning India as a key hub, preparing to introduce an oral version of its experimental weight loss drug orforglipron and a new manufacturing hub in Hyderabad.

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"Classical example of legal illiteracy": IMA on arrest of doctor in child deaths from contaminated cough syrup

The Indian Medical Association has condemned the arrest of a pediatrician in Madhya Pradesh following child deaths from contaminated cough syrup, calling it "legal illiteracy" by police. The IMA demands action against actual culprits and compensation for affected families, emphasizing regulatory failures and the spurious nature of the drug.

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Kerala bars all medicines for children under 12 without prescription

Kerala's Health Department mandated doctor prescriptions for all medicines given to children under 12, citing cough syrup concerns. An expert panel will study cough medicine use to formulate new guidelines. This follows reports of child deaths outside Kerala linked to toxic cough syrups, prompting awareness campaigns and suspension of problematic batches.

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Nanavati Max Hospital inks pact with Namangan Viloyat Republic Hospital in Uzbekistan

Mumbai's Nanavati Max Super Speciality Hospital has partnered with Uzbekistan's Namangan Viloyat Republic Hospital to enhance medical services. This collaboration facilitates knowledge exchange and clinician training in key specialties like multi-organ transplantation, while also providing advanced treatment for Uzbek patients in India. The agreement aims to establish transplant programs and streamline patient care pathways.

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Eli Lilly to invest over $1 billion in India to expand manufacturing capacity

Eli Lilly will invest over $1 billion in India to boost manufacturing and supply through local drugmakers, increasing the availability of key drugs like Mounjaro. This strategic move leverages India's skilled workforce and includes a new Hyderabad facility to oversee contract manufacturing, despite global shifts towards US production.

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Cough syrup issue: Health ministry directs rational use of medication

Union health secretary convened a meeting with states to address drug quality after multiple child deaths linked to contaminated cough syrups like Coldrif, found with DEG/EG. States were directed on rational use, while DGHS advised against prescribing such medicines for children under two, emphasizing careful evaluation for older kids. Probes are underway, and some states have banned the syrups.

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NSE to build Rs 380-crore facility for cancer treatment at Tata Memorial Centre

NSE will build a 380 crore rupee cancer treatment facility at Tata Memorial Hospital. This 11-storey block and bone marrow transplant centre will be in Navi Mumbai. It will serve 1.3 lakh outpatients and conduct over 600 BMTs annually. The facility will have 60 beds. Operations are expected to begin by July 2027.

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India's TB fight gets a boost: New Made-in-India diagnostic tests cut cost & time

India's ICMR has validated two new indigenous TB diagnostic tools from Huwel Lifesciences. The Quantiplus MTB FAST kit offers cheaper, open-system RT-PCR testing on existing machines, while UniAMP MTB uses non-invasive tongue swabs for patient-friendly diagnosis. These innovations promise faster, more accessible, and affordable TB detection, boosting India's elimination efforts.

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Torrent Pharma gets demand notices totalling Rs 6.63 cr from NPPA

Torrent Pharmaceuticals reported receiving demand notices from the NPPA. The notices total over Rs 6.63 crore. They allege overcharging for five drugs between January 2016 and November 2018. The company stated these notices were received on October 3, 2025. Torrent Pharmaceuticals expects no material financial impact from this development.

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Health Ministry confirms Diethylene Glycol beyond permissible limits in Coldrif cough syrup amid child deaths in Raj, MP

The Ministry of Health confirmed Coldrif Cough Syrup from Sresan Pharma's Kanchipuram unit contained diethylene glycol (DEG) above permissible limits, following investigations into child deaths in Madhya Pradesh and Rajasthan. Tamil Nadu banned its sale, halting production. Authorities initiated risk-based inspections and advised against prescribing cough syrup to children under two.

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Tamil Nadu bans ''Coldrif'' cough syrup after child deaths in MP, Rajasthan

Tamil Nadu has banned the sale of 'Coldrif' cough syrup, manufactured by a city-based firm, following suspicions linking it to 11 child deaths in Madhya Pradesh and Rajasthan. Inspections were conducted, and samples are being tested for Diethylene Glycol. The Union Health Ministry also advised against prescribing cough and cold medications for children under two years.

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Isabgol processors threaten to halt purchases from October 6 over GST

Isabgol processors threaten to halt purchases from farmers due to GST ambiguities, locking up capital for over a year. The industry, exporting ₹3,500 crore annually, faces financial stress and slowed exports as unclear classifications force them to pay GST on seeds, despite refunds. They demand government clarification.

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Indian Pharmaceutical Alliance appoints Zydus Lifesciences MD Sharvil Patel as new president

The Indian Pharmaceutical Alliance (IPA) has appointed Sharvil Patel of Zydus Lifesciences as its new President, with Glenn Saldanha of Glenmark as Vice President. This leadership transition occurs as the industry navigates GST reforms and strengthens its global position in specialty medicines. The new team aims to drive innovation, patient access, and quality healthcare solutions.

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IPA names Zydus Lifesciences MD Sharvil Patel as President

Sharvil Patel is the new president of the Indian Pharmaceutical Alliance. He takes over from Samir Mehta. Glenn Saldanha becomes the vice president. The IPA represents 23 national pharmaceutical companies. The new team will build on reforms and breakthroughs. They will focus on innovation, patient access, and quality in healthcare.

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Panacea Biotec gets supply order from UNICEF for oral polio vaccines worth Rs 315 cr

Panacea Biotec has received a long-term supply order from UNICEF. The order is for bivalent oral polio vaccines. It is valued at USD 35.65 million. Supplies will commence from April 2026 and continue until March 2030. This agreement covers vaccine requirements for UNICEF. The company will provide vaccines in 10 and 20 vial presentations.

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Government invites proposals under PRIP scheme for industry, startup projects

The government has invited applications for its Rs 5,000 crore Pharma-MedTech innovation scheme, aiming to support around 300 projects in new medicines, biosimilars, and medical devices. Revised guidelines offer enhanced financial assistance for MSMEs and startups, including higher support for strategic priority areas. Applications opened on October 1 via a digital portal.

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Novo, Lilly weight-loss drugs should be first option obesity treatments, European doctors say

Semaglutide, the active ingredient in Novo's Wegovy and Ozempic, and tirzepatide, sold as Zepbound and Mounjaro by Lilly, are so effective that they should be the first choice in almost all cases when substantial weight loss is necessary, according to a new guideline from the European Association for the Study of Obesity published in Nature Medicine.

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Pricing depends on the country, Bayer looks at affordability: Executive

India has evolved significantly in the clinical trial setting...we have a significant number of patients and trials running in IndiaAshraf Al-Ouf Head, Pharmaceutical Commercial Ops, APAC, Bayer

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'Contaminated' cough syrup linked deaths: NCDS collects water, entomological drug samples

NCDC collected water and entomological drug samples from Madhya Pradesh and Rajasthan after multiple children died of kidney failure, allegedly linked to contaminated cough syrup. These samples will be tested for infectious diseases, while state drug authorities await results from drug sample tests. Six children died in MP and one in Rajasthan, prompting a ban on 19 syrup batches.

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Indian pharma Wockhardt seeks US approval for new drug to treat UTIs

Wockhardt has submitted a New Drug Application to the USFDA for its novel antibacterial agent, Zidebactam-Cefepime injection. This drug targets complicated urinary tract infections, including those caused by multidrug-resistant Gram-negative bacteria. This marks a significant milestone as the first USFDA NDA for a drug fully discovered and developed by an Indian pharmaceutical company, following successful global Phase III trials.

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Bayer seeks approval for key heart drug in India

Pharmaceutical major Bayer has filed for Indian approval of its patented drug finerenone (Kerendia) to treat heart failure patients with LVEF of 40 and above. This move aims to address India's growing early-onset heart disease burden. Already approved for chronic kidney disease, Bayer anticipates approval for this new indication by year-end, following successful trials.

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Global report says 40% of clinicians in India could be using AI in work

Over 40 per cent of Indian clinicians are now using AI for work, a threefold increase from last year, surpassing global adoption rates. Despite this rapid embrace and optimism, challenges like clinician burnout and institutional gaps in AI training and governance remain. Experts urge focused action to translate digital health policies into effective practice.

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To what extent will Trump's tariffs impact Indian pharma? Govt assesses likely cost

Union Commerce ministry says US tariffs on pharma imports will not significantly impact India. India exports generic drugs, less affected by new rules. The nation is diversifying trade to counter US policy shifts. New free trade agreements with EFTA and the UK will boost marine exports. This strategy aims to broaden India's global market reach.

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Managing diabetes early: A smart choice to consider

Early management of type 2 diabetes is crucial in India, where the disease poses a significant health and financial burden. Starting treatment promptly and adopting lifestyle changes can reduce long-term complications like heart disease and kidney failure. Proactive conversations with healthcare providers and adherence to treatment plans are essential for better health outcomes and reduced healthcare costs.

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Lupin subsidiary inks pact to acquire Netherlands-based VISUfarma

Lupin's subsidiary will acquire VISUfarma BV for 190 million euros. This expands Lupin's European business and eye health product range. The acquisition strengthens Lupin's specialty franchise. It will enter the ophthalmology market. The deal is expected to close by late 2025. This transaction will enhance Lupin's growth and margin profile.

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'Indian generics safe, tariffs unwise': Indian pharma association hits back after US tariff concerns

India's pharmaceutical industry, through the IPA, strongly countered US concerns regarding the quality of generic medicines, warning that tariffs would jeopardize America's drug security and increase reliance on China. The IPA cited FDA reports and independent testing affirming Indian facilities' high standards, highlighting billions saved for the US healthcare system.

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Veterinary vaccine firms form association for collaboration with policymakers

India's leading veterinary vaccine manufacturers, including Hester Biosciences and Indian Immunologicals, have formed the Veterinary Vaccine India Manufacturers Association (VVIMA). This new association will serve as the industry's collective voice, aiming to collaborate with policymakers to foster innovation and position India as a global hub for animal vaccine research and production. Rajiv Gandhi leads as President.

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Glenmark, Granules, Zydus recall products in US over manufacturing issues: USFDA

Indian drugmakers Glenmark, Granules India, Sun Pharma, Zydus, and Unichem are recalling various products in the US market due to manufacturing issues. These include CGMP deviations, failed impurity specifications, and label mix-ups, leading to Class I, II, and III recalls initiated from late August to mid-September. The USFDA reported these voluntary actions.

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Highs & Lows: Could the microdosing of psychedelics be a key missing piece in the mental health jigsaw?

A Netflix documentary highlights the re-evaluation of mind-expanding substances like LSD, once banned but now experiencing a scientific renaissance. New research, including a study on pharmaceutical LSD for anxiety, suggests these psychedelics could redefine mental health treatment. However, overcoming public demonization and ensuring rigorous scientific trials are crucial for their widespread acceptance.

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Just like bad medicine...Trump tariff pricks again; India not seen badly hit by US’ latest salvo

US President Trump’s 100% tariff on pharmaceutical products targets only branded and patented drugs, leaving India’s generic exports largely unaffected, experts say. The tariff, effective October 1, spooked pharma stocks but poses minimal immediate risk. India exported $9.8 billion in pharma to the US in FY25. Tariffs on furniture and trucks may benefit India, while bilateral trade talks continue.

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Weight-loss drug Ozempic to debut in India soon

Novo Nordisk will launch Ozempic in India. This injectable drug manages type 2 diabetes and aids weight loss. It enters a competitive market against Eli Lilly's Mounjaro. Novo Nordisk's Wegovy also competes. The company's semaglutide patent expires next year, allowing generic versions. India has a large population with diabetes and obesity. Ozempic offers significant health benefits.

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Diabesity: It’s more than you think

The intertwined rise of obesity and type 2 diabetes, termed 'diabesity,' presents a significant health challenge in India. This condition, driven by complex factors beyond lifestyle, faces stigma hindering effective treatment. Indians, despite appearing thin, often have higher body fat, increasing their risk.

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Trump delivers another bitter tariff pill. Who’s set to bite the dust?

A new tariff announced by President Trump will impose a 100% levy on patented pharmaceuticals entering the U.S. from October 1, 2025, unless companies have manufacturing facilities in the country. This policy raises uncertainties about which drugs will be affected and challenges the Indian pharmaceutical sector, which significantly contributes to the U.S. market—supplying 47% of generics and saving the U.S. healthcare system $219 billion in 2022.

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Trump's 100% tariff on pharma will not impact generic makers, says Indian Pharma Alliance

The Indian Pharmaceutical Alliance clarifies that Trump's proposed 100% tariff targets patented and branded drugs, not generics, potentially impacting a segment of Indian exports. While the immediate effect on Indian exports may be limited due to their focus on generics and existing US manufacturing presence, the industry is advised to prepare for future policy changes and explore advanced pharmaceutical opportunities.

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Meril’s Mizzo Endo 4000 sets a new benchmark in robotic surgery

Meril, an Indian medical device company, has launched the Mizzo Endo 4000, a next-generation surgical robotic system. This advancement aims to enhance surgical precision and accessibility across various specialties. The system features AI-powered 3D mapping, an open console, and 5G-enabled telesurgery.

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Alembic Pharma gets USFDA nod for generic drug to treat depression, anxiety

Alembic Pharmaceuticals Ltd. announced it has secured final approval from the USFDA for its generic Paroxetine extended-release tablets, available in 25 mg and 37.5 mg strengths. These tablets are therapeutically equivalent to Apotex Inc's Paxil CR and indicated for treating major depressive disorder, panic disorder, social anxiety disorder, and premenstrual dysphoric disorder.

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HIV-prevention drug to cost $40 a year from 2027

The two organizations have signed separate agreements with Indian pharmaceutical companies to produce cheaper generics of lenacapavir - a twice-yearly injection shown to reduce the risk of HIV transmission by more than 99.9% - for low- and middle-income countries.

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HCA Healthcare to invest $75 mln to set up Global Capability Center (GCC) in Hyderabad

HCA Healthcare inaugurated its Global Capability Center in Hyderabad, investing USD 75 million by 2025. The center, spanning 400,000 square feet, will employ 3,000 professionals by 2026, focusing on IT, supply chain, and finance. This strategic hub aims to drive innovation and operational excellence, supporting HCA Healthcare's patient care in the US and UK.

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Tata 1mg likely to get $200 mn booster shot; Novo, CPPIB, Permira and ChrysCap line up

Novo Holdings, CPPIB, Permira, and ChrysCapital have shown interest in investing in Tata Group’s online pharmacy 1mg, which seeks up to $200 million for its next growth phase. The investors, however, consider the $1.25 billion 2022 valuation too high, proposing $750–800 million instead. Some also want board seats, which Tata is unwilling to offer.

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India’s liver-heart-diabetes triangle: Why acting early could save your life

In India's bustling cities like Mumbai, a concerning trend emerges as fatty liver disease, now termed MASLD, quietly rises alongside diabetes and heart disease. Sedentary lifestyles, poor diets, and lack of awareness contribute to its prevalence, even among those with normal weight.

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Vidal Health and Serum Institute collaborate on HPV vaccine access

Vidal Health, in partnership with Serum Institute of India, will launch a digital platform on October 1, 2025, to streamline HPV vaccine access and promote cervical cancer prevention. The platform offers convenient appointment booking, digital consent, and certification, ensuring a cashless and paperless experience. This collaboration aims to improve vaccine delivery efficiency and awareness, supporting national healthcare efforts.

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India’s cheap birth control pills in US could vanish under Trump’s 250% tariff threat

Donald Trump's tariff threat jeopardizes affordable Indian medicines in the US. Birth control pills, hypertension, and depression treatments are most vulnerable. India, the world's pharmacy, faces potential export losses. Analysts foresee price hikes and supply chain disruptions. Indian firms may struggle to absorb tariffs. The US aims to boost domestic drug production. This move risks higher drug prices for Americans.

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India’s unique diabetes profile: The Indian diabetes phenotype—why our bodies react differently

Diabetes is rapidly increasing in India, affecting over 101 million people, often manifesting differently than in the West. Indians tend to develop diabetes earlier, even at lower weights, due to a "thin-fat" body type and less muscle mass. Genetic predispositions, poor early-life nutrition, and sedentary lifestyles contribute to this alarming trend, with many unaware of their condition.

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Drug companies flag concerns over timeline for carrying out regulator's manufacturing rule

Small and medium pharmaceutical companies are appealing to the health minister, raising concerns about stringent manufacturing standards imposed by the central drug regulatory body. These associations fear that the abrupt implementation timeline will force many MSMEs to shut down due to financial constraints and inability to meet the new requirements, potentially leading to medicine shortages.

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PE fund KKR closes third buy in Kerala, at Meitra Hospital

KKR, buoyed by its successful Max Healthcare exit, is expanding its hospital investments in South India. Its Kerala-based Baby Memorial Hospital (BMH) has acquired a majority stake in Meitra Hospital for ₹1,000-1,200 crore and is considering acquiring Star Care Hospital.

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Rehabilitation: India's 'missing link' in healthcare

Experts at the IAPMR Mid-Term CME 2025 highlighted India's rehabilitation shortage, emphasizing that discharge is not the end of treatment. The lack of structured rehabilitation, inadequate insurance coverage, and the removal of PMR from the medical curriculum are contributing to delayed recovery and frequent readmissions. They advocate for mandatory rehabilitation protocols and increased awareness to improve patient outcomes.

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India push into global natural healthcare market, government research institutions develop new drugs

India's herbal healthcare sector is preparing for a new growth phase, as traditional medicine blends with modern science to produce validated, affordable, and globally competitive solutions. This momentum was on full display at the recently concluded two-day CSIR Startup Conclave, where research institutions, startups, and policymakers joined forces to demonstrate how herbal formulations are moving from laboratories to the marketplace.

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"Transformative shift in India's healthcare": Pharma alliance lauds GST reforms ahead of implementation

The Indian Pharmaceutical Alliance lauds the upcoming GST reforms, effective Monday, as a transformative step towards affordable healthcare. Prime Minister Modi's initiative reduces GST on most medicines from 12% to 5%, with complete exemption for 36 critical life-saving drugs.

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Healthcare set to be more affordable as new GST rate kicks in from Sep 22: Pharma industry

From September 22, medicines and medical devices in India will become cheaper under new GST rates, making healthcare more affordable, say industry experts. Most drugs’ GST drops from 12% to 5%, while 36 critical life-saving medicines are fully exempt. Tax slabs on insurance, glucometers, and spectacles are also rationalised, easing costs for patients and improving access to essential care.

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Fermenta board approves sale of environmental solutions biz to subsidiary

Fermenta Biotech on Friday said its board has approved transferring its environmental solutions business to a wholly owned subsidiary on a slump sale basis, effective October 1, 2025.

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Fire at subsidiary unit temporarily hits production: Aurobindo Pharma

Aurobindo Pharma reported a fire incident on September 18, 2025, at its APL Healthcare Unit-IV in Andhra Pradesh due to a short circuit, causing temporary production disruption. The fire, contained with no casualties, impacted two out of nineteen lines, resulting in an estimated 3% reduction in monthly capacity. Refurbishment is underway, with operations expected to resume in a few weeks.

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PMO acts on pharma MSMEs 'crisis call'

The PMO has been alerted to potential medicine shortages and price increases due to stringent regulatory actions on pharmaceutical quality. The Federation of Pharma Entrepreneurs warns that many MSMEs face closure due to costly GMP upgrades, potentially impacting the supply of essential medicines and causing significant job losses. They are urging the government to extend the compliance deadline.

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Indian pharma sector to log 7-9% growth in FY26 despite US headwinds: ICRA

India's pharmaceutical industry is set to record healthy revenue growth of 7-9 per cent in FY26, even as challenges in the United States market continue to weigh on performance, noted rating agency ICRA in its latest sector outlook.

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Natco Pharma's Kothur unit classified as 'voluntary action indicated' by US regulator

Natco Pharma Ltd announced that its Kothur unit in Hyderabad received an Establishment Inspection Report (EIR) from the US FDA, classifying the facility as 'Voluntary Action Indicated' (VAI). The US FDA had previously conducted an inspection of the company's pharma division at the Kothur location. While objectionable conditions were noted, the agency does not plan immediate regulatory action.

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India ranks among top contributors in reporting adverse events: Drugs Controller General of India

DCGI Dr. Rajeev Raghuvanshi highlighted India's leading role in global adverse event reporting during the 5th National Pharmacovigilance Week. The week-long campaign, themed 'Your Safety, Just a Click Away: Report to PvPI', aims to encourage ADR reporting through simplified digital platforms.

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AstraZeneca's asthma drug fails 'smoker's lung' study

AstraZeneca's Fasenra failed to reduce flare-ups in COPD patients in a late-stage trial, a setback for the company's efforts to address the severe lung disease. Despite this, AstraZeneca will analyze the data to understand the results better, while its rare disease drug Saphnelo succeeded in a lupus trial.

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'Nimesulide' may come with warning label

Indian drug regulators have mandated cautionary labels for nimesulide, restricting its use as a second-line treatment for patients 12 years and older after exhausting first-line options. The labels must warn against use during pregnancy, lactation, or by women planning pregnancy, as well as in patients with renal or hepatic impairment.

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Novo Nordisk to test weight-loss drugs in broader range of obesity-linked conditions

Novo Nordisk is broadening its focus beyond obesity and diabetes by exploring the potential of its weight-loss drugs, including Wegovy, to treat conditions like knee osteoarthritis and sleep apnea. Clinical trials are planned to investigate the impact of CagriSema and amycretin on various obesity-related comorbidities.

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Scheme to promote innovation in pharma, medtech sectors to be launched this month: Pharma Secretary

The government will soon launch a scheme to boost innovation in the pharmaceutical and medical technology sectors. The PRIP scheme has a financial outlay of Rs 5,000 crore. It will support research and development. The scheme aims to reduce reliance on imports. Three medical device parks are expected to be functional by early 2027.

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In major move, patent of Novartis' blockbuster cardiac drug revoked by India

The Indian Patent Office revoked Novartis' patent for Vymada, a heart failure drug, citing a lack of novelty and inventive step. This decision paves the way for generic versions, potentially lowering treatment costs for Indian patients. Domestic pharmaceutical companies had challenged the patent, arguing it violated Section 3(d) of the Patents Act, which prevents 'evergreening'.

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Novo Holdings in talks to buy into Surya Hospitals

Novo Holdings is in exclusive discussions to acquire a 49% stake in Surya Hospitals, valuing the Mumbai-based chain at ₹1,000 crore. This potential deal highlights the increasing consolidation in India's hospital sector, driven by significant financial investor activity.

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India’s heart-risk score in diabetes: Why every Indian must pay attention - A World Heart Month special

In India, individuals with diabetes face a significant risk of cardiovascular disease, necessitating proactive heart health management. Tools like the IDRS and QRISK3 Score help assess this risk, especially crucial given the early onset of heart disease in Indians. Vigilance through regular check-ups, lifestyle adjustments, and awareness during World Heart Month can significantly improve outcomes.

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Roche Pharma partners with 10 govt hospitals to bolster clinical trial capabilities in India

Roche Pharma collaborates with ten government hospitals. The goal is to improve clinical trial capabilities across India. Nearly 400 professionals receive training based on global standards. This initiative helps bring innovations to India faster. It aligns with priorities to boost government site participation. The Advanced Inclusive Research Site Alliance is now active in India.

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Reckitt has joined hands with PATH-CHRI to Launch Dettol Banega Swasth India - Maternal and Child Health Tech Accelerator.

Reckitt, in collaboration with PATH-CHRI, has launched an accelerator to drive innovation in maternal and child health. Centred on the first 1,000 days of life, the initiative aims to improve outcomes and strengthen India’s progress toward Viksit Bharat @2047.

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Why Indians skip the flu vaccine despite risks

In India, the quadrivalent influenza vaccine (QIV) faces low uptake due to limited awareness and high costs, despite being recommended for vulnerable groups. While global guidelines promote annual flu shots, India's lack of inclusion in the Universal Immunization Programme contributes to poor vaccination rates. Experts emphasize that yearly vaccination is necessary, although not foolproof, to mitigate flu severity and complications.

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Creador to buy 7% stake in pharma company La Renon

Creador, a Kuala Lumpur-based private equity firm, is set to acquire a 7% stake in La Renon Healthcare for ₹800 crore, valuing the Indian pharmaceutical company at nearly ₹11,000 crore. The transaction involves a partial stake dilution by the promoter family and Peak XV Partners.

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Pharma exporters seek rollback of rule banning export of India-only drugs

A new regulation by India's drug authority, restricting the export of pharmaceuticals labeled "For sale in India only," is causing significant losses to exporters, estimated at $500 million, and limiting access to affordable medicines for patients abroad.

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Cupid announces strategic investment in fragrance brand Mansam

Cupid Ltd, an Indian healthcare products manufacturer, has signed a term sheet to acquire a strategic stake in Mansam, a Saudi Arabian luxury fragrance brand. The investment, facilitated through a fund managed by GII Investment Management Limited, aims to expand Cupid's international presence and tap into new consumer-driven markets.

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Biocon inaugurates first manufacturing facility in US

Biocon Ltd has inaugurated its first US manufacturing facility in Cranbury, New Jersey, operated by its subsidiary, Biocon Generics Inc. Following the acquisition of the Oral Solid Dosage facility from Eywa Pharma Inc in 2023, Biocon invested over USD 30 million to establish the plant.

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Dr Reddy's inks pact with Johnson & Johnson to acquire vertigo treatment brand

Dr. Reddy's Laboratories has finalized its acquisition of the Stugeron brand from Johnson & Johnson, encompassing EMEA regions, India, and Vietnam. This strategic move allows Dr. Reddy's to broaden its presence in the anti-vertigo market and reinforce its Central Nervous System portfolio. The company aims to extend Stugeron's reach across 18 key markets, aligning with its goal of reaching 1.

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Delhi HC stops drug body from taking action against IndiaMart

The Delhi High Court has temporarily blocked the CDSCO from pursuing criminal action against IndiaMart for allegedly listing unapproved medicines. This decision follows complaints regarding the online marketplace listing drugs like Crysvita, Oxbryta, and Jynneos, which are not approved for sale in India.

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Indian hospitals to raise IT innovation spend by 25% in 3 years: Report

Indian hospitals are poised to significantly increase their IT innovation spending, with a large portion of healthcare providers already dedicating a substantial part of their IT budgets to digital advancements. The focus will be on enhancing patient experience, improving clinical outcomes through technology, and enabling data-driven decision-making.

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WHO adds popular weight-loss drugs to essential medicines list

The World Health Organization has included Semaglutide and Tirzepatide, popular weight-loss drugs, in its Model List of Essential Medicines. This decision could significantly lower the prices of these medications in countries like India, where obesity rates have surged. The WHO aims to improve access and health outcomes by prioritizing those in need and encouraging generic competition.

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Medicines may soon come with braille labels, audio QR codes

India's drug regulatory authority is exploring the addition of braille cards and voice-assisted QR codes on medicine strips to improve accessibility for visually impaired individuals. This initiative follows representations highlighting the difficulties faced by blind individuals in identifying medicines.

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Indian pharma sector needs price hikes, site and IP transfers to tackle US tariff uncertainty: Report

A Systematix Research report indicates the Indian pharmaceutical industry is navigating uncertainty due to US tariffs, necessitating price increases, site transfers, and IP transfers. While raw material prices stabilize and companies explore new growth avenues, first quarter earnings were weak, with margin pressures in the US market. Firms cautiously evaluate inorganic growth and focus on OTC platforms amid these challenges.

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The missed window: Why half of India’s people with diabetes learn too late

Many Indians unknowingly live with diabetes, missing the crucial early detection window. This delay, often due to subtle symptoms and lifestyle factors, leads to severe complications like kidney damage and heart issues. Early screening, awareness of risk factors, and regular check-ups are vital to managing diabetes and preventing long-term health problems.

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Health experts alarmed by GST cut on beedis, demand uniform taxation

Health experts have criticised the government’s move to cut GST on beedis from 28% to 18% while keeping other tobacco products at 40%. They warned cheaper beedis, widely used by poor communities, could worsen India’s tobacco burden. Doctors stressed beedis are as harmful as cigarettes, urging uniform high taxes to curb use, protect vulnerable groups, and reduce health costs.

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AstraZeneca to invest Rs 176 cr to expand GITC in Chennai

AstraZeneca is investing Rs 176 crore to expand its Global Innovation & Technology Centre in Chennai, marking its third investment in India in two years. This expansion will enhance the center's capabilities in AI, data analytics, and machine learning, supporting the development of next-generation medicines and digital healthcare solutions.

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USFDA issues Form 483 with 8 observations to Aurobindo's Telangana unit

Aurobindo Pharma faces scrutiny. The US FDA inspected its Bachupally, Telangana plant. The inspection occurred between August 25 and September 5. Following the inspection, the US FDA issued a Form 483. The form contained eight observations. Aurobindo Pharma stated the observations are procedural. The company plans to respond to the US FDA within the given timeframe.

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Glenmark initiates multi-nation Phase 3 clinical trial for lung cancer drug

Glenmark Pharmaceuticals has commenced a Phase 3 clinical trial across multiple countries, including India, Russia, Brazil, and Mexico, for Envafolimab, a novel drug targeting third-stage non-small cell lung cancer (NSCLC). The trial aims to evaluate the drug's efficacy, safety, and other key parameters in NSCLC patients.

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Type 2 diabetes triggering heart attacks in the 30s: Why India’s youth are at risk?

Type 2 diabetes is increasingly affecting young Indians, accelerating heart disease risks due to factors like genetics, visceral fat, and unhealthy lifestyles. Modern diets high in fats and sugars, coupled with sedentary habits and mental stress, significantly contribute to early heart attacks.

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Pharma companies cheer lower drug prices, API tax gap stirs worry

Goods and Services Tax reforms are expected to reduce medicine prices in India. Experts say this will benefit patients and businesses. However, concerns exist regarding the higher tax rate on Active Pharmaceutical Ingredients. This could increase working capital pressure, especially for smaller companies. Provisional refunds may help mitigate these challenges. The government has reduced GST on several expensive medicines.

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GST cut on drugs, medical devices to provide relief to patients: Industry players

The government is reducing GST on medicines and medical devices. Lifesaving drugs are exempt. This action will help patients and families. It will also make healthcare more affordable. Sudarshan Jain and Anil Matai welcome the changes. Ameera Shah and Shobana Kamineni also support the move. Himanshu Baid says it will improve access to medical technologies.

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Crucial drugs to be more affordable after GST cut

The government has significantly reduced GST rates on 41 highly priced medicines, including those for cancer, rare diseases, and heart conditions, aiming to make healthcare more affordable. Key drugs like Risdiplam and daratumumab will now have zero GST, benefiting patients with spinal muscular atrophy and multiple myeloma.

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Centre set to amend rules to simplify drug testing process

The Indian government is amending drug regulations to expedite the approval process for clinical trials and bioavailability/bioequivalence studies. These changes aim to reduce the statutory processing time for test license applications from 90 to 45 days. By simplifying procedures and reducing the number of license applications, the government anticipates faster drug development and approval, benefiting stakeholders and optimizing resource allocation.

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Alkem's Enzene powers into US with $70 m investment

Enzene Biosciences, an Alkem Labs subsidiary, has inaugurated a new US manufacturing plant. The facility is located in New Jersey. This venture represents a $70 million investment. It aligns with calls to boost local pharma manufacturing. Enzene's technology offers cost-effective drug production. The company currently employs 50 people. Enzene plans to increase its workforce to 200.

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Singapore-based firm proposes to acquire 25% in Welcure Drugs & Pharma

Welcure Drugs & Pharmaceuticals receives an offer from Telexcell Trade. Telexcell Trade, based in Singapore, plans to acquire a 25 per cent stake. The indicative price is Rs 20 per share. This investment aims to expand Welcure's global presence. The all-cash investment is estimated at Rs 52 crore. Welcure intends to invest in an agro-pharma research lab.

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Lupin gets USFDA nod for generic risperidone extended-release injectable suspension

Lupin Ltd. secured USFDA approval for its generic risperidone extended-release injectable suspension, a treatment for schizophrenia and bipolar disorder. This marks Lupin's first product utilizing Nanomi BV's technology, benefiting from 180-day competitive generic therapies exclusivity. The drug, with estimated annual sales of USD 190 million, expands access to complex injectables for patients globally.

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Caplin Point arm gets USFDA nod for milrinone lactate in 5 pc dextrose injection

Caplin Point Laboratories' arm, Caplin Steriles, secured USFDA approval for its generic milrinone lactate in 5% dextrose injection. Indicated for acute decompensated heart failure, the injection is a generic version of Sanofi Aventis' PRIMACOR. The US market for this injection reached approximately USD 11 million in sales for the year ending July 2025.

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Medical device manufacturers allowed to give free samples

Medical device companies in New Delhi can now give doctors free samples. There are rules for this. The sample's price must match what stockists pay. If the company bought the sample, that price counts. Company CEOs must ensure code compliance. Marketing costs must be disclosed yearly. This promotes ethical marketing and benefits both manufacturers and patients in India.

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India eyes Russia, Brazil, Netherlands for pharma export growth as US tariffs concerns linger

India is strategically planning to boost its pharmaceutical exports to Russia, the Netherlands, and Brazil, aiming to reduce reliance on the U.S. market due to tariff concerns. While the U.S. remains a crucial market, India seeks to diversify its export chain and increase market share in these growing regions.

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Glenmark launches generic cancer treatment drug in US

Glenmark Pharmaceuticals on Tuesday launched Eribulin Mesylate Injection, a generic cancer treatment, in the US through its subsidiary Glenmark Pharmaceuticals Inc., USA. The product, equivalent to Eisai’s Halaven Injection, will begin distribution this month.

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Zydus launches VaxiFluTM trivalent influenza vaccine for flu protection in India

Zydus Lifesciences has introduced VaxiFlu, a trivalent influenza vaccine, in India. This vaccine aligns with WHO guidelines. It is for individuals aged six months and above. The vaccine contains updated strains for optimal protection. Flu remains a global health concern. It causes millions of severe illnesses and respiratory deaths annually. VaxiFlu aims to reduce vaccine-preventable diseases, especially in high-risk groups.

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Fortis Healthcare arm inks 15-year lease with RR Lifesciences to expand NCR reach

Fortis Healthcare's subsidiary, International Hospital Limited, has secured a 15-year lease. This agreement with RR Lifesciences Limited allows Fortis to operate and expand its facility in Greater Noida. Fortis will now have complete control over the 200-bed hospital, known as Fortis Hospital Greater Noida. The hospital aims to increase its capacity to approximately 250 beds.

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The #WeightofDiabetes iceberg: Why the real burden lies beneath the surface

India faces a significant diabetes crisis, with millions undiagnosed, increasing the risk of heart disease. Early detection through screening and lifestyle changes like diet and exercise are crucial. Community programs and modern treatments offer hope for managing diabetes and improving long-term health outcomes, reducing the economic and health burden.

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Govt launches advanced biomanufacturing hubs to boost bioeconomy, innovation

India has launched a network of advanced biomanufacturing hubs to boost its bioeconomy and drive innovation across sectors like health, agriculture and energy. This initiative, under the BioE3 Policy, provides state-of-the-art infrastructure and expertise to startups and researchers. India aims to achieve a USD 300 billion bioeconomy by 2030, positioning itself as a global leader in biotechnology.

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Novo Nordisk ties up with Apollo Clinics for obesity management initiative

Novo Nordisk partners with Apollo Clinics to tackle obesity in India. The collaboration introduces a comprehensive obesity management programme across Indian cities. This initiative aims to provide structured care through multiple levels. The partnership focuses on equipping healthcare professionals with tools and support. The goal is to deliver personalized, evidence-based interventions.

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Pharmaceutical industry seeks relief from rate inversion

The pharmaceutical industry in India anticipates potential relief from Goods and Services Tax inversion. Discussions between companies and the government suggest a favourable resolution within upcoming GST reforms. The current tax structure creates working capital issues, especially for MSMEs. Delayed refunds force MSMEs to take loans. Exporters face strain paying upfront taxes on APIs.

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Indian hospitals battle central line infections linked to mismanagement of tubes used for administering medicines and fluids

A seven-year Indian study reveals alarmingly high rates of bloodstream infections from central lines, especially in newborns, with a 40% mortality rate within two weeks. The infection rate is significantly higher than in the US, exacerbated by antibiotic resistance and overwhelmed ICUs during COVID-19. Experts emphasize the need for improved monitoring, infection control, and staffing to reduce these preventable infections.

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Repurposed anti-cholesterol drug statin can stymie cancer, help support treatment, say researchers

Statins, drugs for high cholesterol, show promise in slowing colorectal cancer growth. Researchers at Shiv Nadar University and IISER Pune found statins target key pathways in cancer cells. The study suggests statins could be repurposed for cancer treatment. More trials are needed to confirm these findings.

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Scientists find why ultra-processed diets make you gain fat even without extra calories: Study

A recent study reveals that consuming ultra-processed foods leads to greater weight gain compared to minimally processed diets, even with the same calorie intake. The research, involving healthy young men, also found that ultra-processed diets disrupt hormone levels and introduce pollutants linked to decreased sperm quality. These findings underscore the detrimental impact of processed foods on metabolic and reproductive health.

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Zydus Saroglitazar shows positive Phase 3 results in rare liver disease PBC, US filing planned in 2026

Zydus Therapeutics reveals encouraging outcomes from Saroglitazar's clinical trial. The drug targets Primary Biliary Cholangitis. The EPICS-III trial demonstrates improved liver function in patients. These patients did not respond to standard treatment. Zydus plans to seek US regulatory approval in early 2026. Saroglitazar is a novel treatment option. It addresses bile acid toxicity and liver inflammation.

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Murae Organisor plans to boost agro-sector presence under Rs 80-cr investment strategy

Murae Organisor Ltd is set to bolster its agro-sector presence with an Rs 80 crore investment in R&D and infrastructure. The plan includes establishing an Agro R&D Laboratory, developing processing and packaging infrastructure, and implementing digital traceability systems. This strategic move follows the company's proposed qualified institutional placement (QIP) of up to Rs 80 crore.

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IHH Healthcare to add 2,000 beds in India by 2028

IHH Healthcare plans to expand its presence in India by adding approximately 2,000 new beds by 2028. This expansion will be facilitated through its subsidiaries, Fortis Healthcare and Gleneagles Healthcare, which currently operate 35 hospitals with over 5,000 beds across 11 states.

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FDA approves updated COVID-19 shots but limits access for some kids and adults

U.S. regulators have approved updated COVID-19 shots from Pfizer, Moderna, and Novavax, but access is now limited for younger adults and children to those with high-risk conditions. Pfizer's vaccine is no longer available for children under 5, while Novavax's shot is restricted to those 12 and older. These changes reflect a shift in U.S.

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Catching heart disease in its quietest moments in Type 2 diabetes

Early detection of heart disease in Type 2 diabetes is crucial, as it often develops silently. Advanced tests like high-sensitivity blood work, imaging, and genetic screening can identify hidden risks before symptoms appear. Proactive measures, including lifestyle changes and personalized medication, can significantly reduce cardiovascular complications and improve outcomes.

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Drug, medtech companies fear GST changes may squeeze funds

Pharma and medtech sectors are concerned about upcoming Goods and Services Tax changes. They anticipate higher operating costs and working capital issues. Rajiv Nath suggests a balanced GST approach for equipment and consumables. Federation of Pharma Entrepreneurs urges lower GST on APIs to avoid inverted duty structure. MSMEs fear blocked funds and slowed growth due to tax imbalances.

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Dr Reddy's expects new GST framework to address critical issues impacting pharma sector

Dr Reddy's Laboratories anticipates that the new Goods and Services Tax structure will address existing challenges. It will also create a rationalised tax framework for the pharmaceutical sector. The Association of Indian Medical Device Industry seeks to retain 12 percent GST for most consumables. It also wants 5 percent rate on costly equipment.

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Dr Reddy's launches novel drug for chronic constipation management

Dr Reddy's Laboratories has introduced Colozo, a generic drug for chronic constipation in India. This medication, Linaclotide, is approved by the USFDA. It addresses chronic idiopathic constipation and irritable bowel syndrome. This launch strengthens Dr Reddy's gastrointestinal segment. It follows the introduction of BixiBat in India last year. The company aims to improve patient care and serve 1.

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Sampre Nutrition inks 3-year manufacturing pact with Rama Exports for nutraceuticals

Sampre Nutrition has partnered with Rama Exports in a manufacturing agreement to produce nutraceuticals and food products. Sampre Nutrition will handle manufacturing, supply, quality assurance, and packaging, while Rama Exports will purchase the finished goods over a three-year contract. This agreement is projected to generate Rs 15 crore in business, boosting Sampre Nutrition's revenue and strengthening its operations.

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GSK enters into oncology segment; launches therapies for gynaecological cancers

GlaxoSmithKline Pharmaceuticals has entered the oncology segment in India, introducing Jemperli and Zejula for gynaecological cancers. These therapies address unmet needs in endometrial and ovarian cancer treatment, with incidence projected to rise significantly by 2045. Jemperli offers targeted immunotherapy for advanced endometrial cancer, while Zejula provides first-line maintenance therapy for advanced ovarian cancer.

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From Clinic to Crisis: How Poor Follow-Up Fuels the Type 2 Diabetes Epidemic

Many individuals with diabetes in India are unaware of their condition, leading to missed opportunities for early treatment and increased health risks. Regular follow-up appointments are crucial for monitoring progress, identifying early warning signs, and adjusting treatment plans to prevent complications. Skipping these check-ups can result in silent damage to vital organs and faster progression of the disease.

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India's healthcare chains set their hearts on foreign patients

Indian healthcare providers are aggressively pursuing a larger share of the medical tourism market, fueled by a significant increase in foreign patients seeking treatment. Tourist arrivals for medical reasons have surged, with hospitals now attracting patients from Europe and the UK, in addition to traditional markets.

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Global PE firms tighten grip on India’s $80-billion hospital sector

India's private hospital sector has seen a significant shift towards ownership by global private equity firms in the last five years, especially after the Covid-19 pandemic. This trend is reshaping the healthcare market, attracting investments from entities like Temasek, TPG, and KKR.

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IMA warns of misuse, mis-prescription of new weight-loss drugs, such as Wegovy and Mounjaro

The Indian Medical Association is raising concerns about the misuse of weight-loss drugs like Wegovy and Mounjaro, urging stricter prescription controls. They plan to petition the health ministry and drug regulator, advocating for prescriptions to be limited to certified endocrinologists or diabetologists. Rampant prescriptions by cosmetologists and other non-specialists are fueling concerns about potential side effects and improper usage.

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Novo Nordisk warns patients after theft of weight-loss, diabetes drugs

Novo Nordisk urges customers to purchase medications solely from authorized pharmacies with valid prescriptions after a theft of products, including semaglutide and insulin treatments, during transportation. The company is cooperating with authorities and reinforcing supply chain safeguards. CDSCO has issued an alert, advising caution and vigilance in procuring Novo Nordisk products from trusted sources due to potential compromised quality.

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CDSCO issues alert on Novo drugs after reported theft

The CDSCO has alerted healthcare professionals and consumers about stolen Novo Nordisk products, including semaglutide and insulin injectables. These products, requiring specific temperature control (2-8°C), may be compromised if improperly stored. The regulator has instructed state drug control offices to monitor the market and take action under the Drugs and Cosmetics Act, 1940, while police investigate the theft during transit.

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Substantial cancer drugs beyond ambit of current price control mechanisms: Parliamentary panel

A parliamentary panel has urged for broader price controls on cancer drugs, noting that many remain unaffordable. The committee recommends regular market assessments, quality monitoring of generic medicines, and enhanced domestic research. Streamlining regulatory pathways and fostering public-private collaboration are crucial for improving access to novel therapies.

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Stricter shelf life rule a bitter pill to swallow for pharma companies

A new regulation by the CDSCO mandates that exported drugs must have at least 60% shelf life remaining, causing significant losses to the Indian pharmaceutical industry. Manufacturers are now forced to destroy stocks to comply with this rule. The industry is urging for a revision, citing unnecessary losses and questioning the need when importing countries permit shorter shelf lives.

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Drugmaker Novo Nordisk freezes hiring for non-critical jobs

Novo Nordisk, the maker of Wegovy, has initiated a global hiring freeze for non-critical roles amid increasing competition and pressure from Eli Lilly. This decision follows a profit warning that led to a significant drop in market value and the appointment of a new CEO, Mike Doustdar, who is considering cost-saving measures, including potential layoffs.

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Natco Pharma launches generic drug with 180-day exclusivity in US

Natco Pharma has launched Bosentan tablets, a generic version of Tracleer, in the US for treating pulmonary arterial hypertension in young patients. This launch comes with 180-day exclusivity. Lupin Ltd. is Natco's marketing partner for this product. The drug had estimated sales of USD 10 million in the US for the 12 months ended June this year.

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When the heart and sugar collide: The overlooked risk in Type 2 diabetes

Type 2 diabetes significantly elevates the risk of heart disease due to high blood sugar damaging arteries, leading to plaque buildup and reduced blood flow. Recognizing subtle symptoms like chest pain or shortness of breath is crucial for early intervention. Simple lifestyle adjustments, including a balanced diet, regular exercise, and stress management, can significantly protect heart health.

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Aurobindo Pharma closing in on $5.5b Zentiva buyout

Largest Indian pharma M&A in final lap; PE firm GTCR only other contender. A portfolio company of Advent International, Zentiva will significantly boost Aurobindo’s European footprint.

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Indian drugmakers seek exemption for generics from US supplies probe

Indian pharmaceutical industry representatives met with Union Commerce Minister Piyush Goyal. They requested the US government to exclude generic drugs from its investigation into pharmaceutical imports. The probe, under Section 232, raises concerns about supply chain disruptions. This discussion occurs amidst India-US trade negotiations and potential US tariffs.

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Glenmark, Alembic Pharma, Sun Pharma recall products in US: USFDA

Glenmark, Alembic Pharmaceuticals, and Sun Pharma are recalling various products in the US due to manufacturing issues, according to the USFDA. Glenmark is recalling Carvedilol tablets due to nitrosamine impurity and Theophylline tablets for failed dissolution. Alembic is recalling Doxepin capsules for a similar impurity issue, while Sun Pharma recalls Spironolactone tablets due to aluminum contamination.

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Alembic gets USFDA nod for generic drug for skin condition

Alembic Pharmaceuticals has secured USFDA approval for its generic Tretinoin Cream USP (0.025%), a treatment for acne vulgaris. This ANDA is therapeutically equivalent to Bausch Health US, LLC's Retin-A Cream. The market size for Tretinoin cream USP (0.025%) is estimated at USD 94 million for the twelve months ending June 2025.

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Aurobindo Pharma expects China plant to break even at EBITDA level this year

Aurobindo Pharma anticipates its China facility will achieve break-even by Q3 FY26. Production is ramping up after commencing operations in November 2024. The company invested USD 145 million in the facility. Aurobindo Pharma also invested in US facilities and plans to file for products in the US and Europe.

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Food Chained: How weight-loss drugs are changing India’s eating habits and forcing restaurants to take note

New diabetes and obesity drugs, like Mounjaro and Ozempic, are changing people's relationships with food. While these drugs help control diabetes and promote weight loss by altering taste and reducing hunger, some users experience a loss of enjoyment in eating and even develop food anxieties.

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Max Healthcare to nearly double capacity to 9,500 beds by 2028 after strong quarterly growth

Max Healthcare Institute aims to nearly double its bed capacity to 9,500 by 2028 through brownfield and greenfield expansions, following a 35% increase to 5,000 beds last year. The company reported a 27% jump in first-quarter revenue to Rs 2,574 crore and a 17% rise in net profit to Rs 345 crore, driven by higher occupancy and international patient revenue.

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Cohance Lifesciences announces $10 million investment in US-based arm

Cohance Lifesciences is investing USD 10 million to expand bioconjugation capabilities at its US subsidiary, NJ Bio, enhancing its ADC solutions. This investment aims to support innovators from early development through late-phase clinical supply. Additionally, Cohance is investing Rs 23 crore in a new oligonucleotide building block manufacturing facility in Hyderabad, part of a broader capacity expansion program.

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From burden to breakthrough: Reimagining the #WeightofDiabetes through meaningful conversations with your doctor

Effectively managing type 2 diabetes involves more than just medication; it requires open communication with healthcare providers to address weight, heart health, and emotional well-being. Proactive conversations can clarify confusion, uncover barriers, and empower individuals to take charge of their health, preventing crises and promoting resilience through personalized care and support.

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Intas Pharma completes acquisition of UDENYCA biosimilar for $558 million

Intas Pharma finalized its acquisition of UDENYCA, a biosimilar to Neulasta, from Coherus Life Sciences for $558 million in December 2024. This acquisition strengthens Intas's position as a global leader in pegfilgrastim. Accord BioPharma, Intas's U.S. specialty business, will continue commercializing UDENYCA to reduce infection risk in cancer patients undergoing myelosuppressive chemotherapy.

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Lupin ties up with Sandoz to commercialise biosimilar product

Lupin has partnered with Sandoz Group AG to commercialize its biosimilar ranibizumab across multiple regions, with Sandoz handling commercialization in the EU (excluding Germany), Switzerland, Norway, Australia, Hong Kong, Vietnam, and Malaysia. Lupin will manufacture the product and manage regulatory submissions. Sandoz also gains exclusive rights for commercialization in Canada.

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Chemists seek ban on quick commerce sale of prescription drugs

The All India Organisation of Chemists and Druggists (AIOCD) has appealed to Amit Shah. They want immediate action against e-pharmacies and quick commerce platforms. These platforms are selling prescription medicines online. AIOCD says this poses a public health risk. They are concerned about drug abuse, especially among young people. AIOCD also highlights the issue of ghost prescriptions.

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Asia Healthcare Holdings to invest Rs 400 crore in Asian Institute of Nephrology and Urology to double hospital network

Asia Healthcare Holdings will invest Rs 400 crore in Asian Institute of Nephrology and Urology. The investment will occur over the next 4-5 years. AINU plans to expand by opening 13 hospitals in Tier 2 cities. This expansion includes cities like Patna and Bhubaneshwar. The total investment will reach Rs 1,000 crore by FY30.

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Pfizer launches next-gen vaccine for pneumococcal disease

Pfizer has introduced its 20-valent pneumococcal conjugate vaccine (PCV20) for adults in India, offering protection against 20 serotypes responsible for a majority of pneumococcal diseases. This single-dose vaccine provides timely and proactive protection for all adults, including those with chronic conditions, potentially eliminating the need for a second dose.

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Welcure Drugs & Pharma board to consider share split, bonus issue this month

Welcure Drugs & Pharmaceuticals is set to consider a stock split of 1:10 and a bonus issue of 1:1 in its upcoming board meeting on August 22. This decision follows strong financial results in Q1 FY26, with revenue from operations reaching Rs 299.91 crore and net profit surging to Rs 23.29 crore.

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Zydus Lifesciences gets USFDA approval for angina, high blood pressure drug

Zydus Lifesciences has secured USFDA approval to market Diltiazem Hydrochloride tablets, used for treating angina and high blood pressure, in strengths of 30 mg, 60 mg, 90 mg, and 120 mg. The medication, a calcium-channel blocker, relaxes blood vessels, easing the heart's workload and improving blood flow.

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Retinal disorders a public health crisis, need immediate prioritisation, say experts

Mission Vision, a public health initiative, has launched in India to combat the escalating crisis of vision loss due to Diabetic Retinopathy. The initiative aims to increase awareness, improve screening and treatment access, and integrate eye care into routine diabetes management.

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Managing diabetes in a country obsessed with quick fixes: A scientific perspective

Diabetes management faces challenges due to patients' preference for quick fixes over sustainable lifestyle changes. These shortcuts, like extra medication or unproven supplements, offer temporary relief but neglect long-term disease control. Shifting mindsets requires holistic approaches, personalized support, and collaborative healthcare to promote lasting healthy habits and prevent complications.

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Govt gives BIS exemption to parts used in medical devices for now

The steel ministry has temporarily suspended its notification requiring Indian standards compliance for raw materials used in medical device manufacturing, offering relief to the industry. They will issue no-objection certificates for importing special stainless steel grades and allow foreign suppliers six months to obtain Bureau of Indian Standards registration.

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Biocon sees GLP-1 weight-loss therapy as a future growth driver

Biocon will strengthen its insulin business while advancing in GLP-1 therapies, with semaglutide in Phase-III trials and a planned 2027 India launch. CEO Shreehas Tambe said both portfolios are complementary. Biocon aims to leverage its insulin experience for GLP-1 success, following US FDA approval for insulin aspart and India approval for liraglutide. External risks remain a key concern.

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Medical device firms sound the alarm over new steel standards

Earlier, foreign suppliers only needed BIS certification for finished steel products. Under the new rule, materials like hot rolled steel, ingots manufactured by other countries for Indian buyers will have to get BIS certification. The manufacturers have written to the ministry of steel seeking exemption for the import of stainless steel capillary without BIS certification.

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Weight-loss drug Mounjaro crosses Rs 100 crore sales in 4 months

The drug clocked Rs 47-crore sales in July, double its June figure, according to data from prescriptions tracker PharmaTrac. If this month-on-month doubling of sales continues, Mounjaro’s revenue could cross Rs 500 crore by March, experts estimate.

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Novo Nordisk's Wegovy, Mounjaro sales in India double on month in July

Sales of Novo Nordisk's Wegovy and Eli Lilly's Mounjaro in India doubled in July, according to Pharmarack data. Wegovy, launched in June, saw sales more than double to 5,000 units, while Mounjaro sales also doubled to 157,000 units. Mounjaro's sales have soared 15 times since its March launch in India.

from Healthcare/Biotech-Industry-Economic Times https://ift.tt/AhPSKaq
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