Ambuja Neotia Group to develop over Rs 700 cr integrated healthcare and hospitality project in Guwahati

Ambuja Neotia Group will build a large integrated healthcare and hospitality project in Guwahati. The Rs 700 crore investment will include a 300-bed multi-speciality hospital and a 4+ star hotel. This initiative aims to boost the region's healthcare infrastructure and economy. The project is expected to create thousands of jobs. It marks the group's second healthcare venture in Assam.

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'India has intellectual power to be a leader in biomedical innovation,' says Bayer AG

Bayer's CEO Bill Anderson believes India can become a top pharmaceutical market. He highlights the need for supportive policy frameworks, including stronger intellectual property protection. This will attract investment in cutting-edge drugs. India's young population and technological leadership offer significant opportunities. Bayer is investing in innovation centers in Bengaluru, leveraging Indian talent for global missions.

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India warns drugmakers against direct or surrogate weight-loss drug and obesity ads

India's drug regulator has issued a stern warning to pharmaceutical companies. Direct or indirect advertising of weight-loss medicines is now prohibited. Obesity awareness campaigns that promote prescription drugs are also under scrutiny. This move comes as global and domestic companies vie for a share of India's growing obesity drug market. The regulator emphasizes that misleading promotions will face action.

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India medical device shortage: Polypropylene price surge threatens syringes, IV bags amid Iran war

India's medical devices industry faces a polypropylene shortage due to the Iran war, causing a sharp price increase of over Rs 55 per kg. This surge, coupled with a deepening gas supply crisis impacting syringe production, threatens small and medium enterprises and overall healthcare delivery.

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Govt cautions pharma cos against surrogate ads for promoting GLP-1 drugs

Weight loss drug risks: The government has warned of strict regulatory action against those found using surrogate advertising to promote GLP-1 drugs. "A detailed advisory on the use of GLP-1 drugs is expected to be released in the next few days," sources told ET.

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Decoding the antibiotic resistance crisis: How everyday habits can save our strongest medicines

Antibiotics are losing their power as germs grow stronger, a crisis fueled by everyday misuse. Experts urge parents to rethink treating minor ailments and fevers without medical advice. Preventing infections through simple hygiene practices like handwashing and sanitizing surfaces, summarized by the S.H.A.K.E. formula, is crucial to preserving these life-saving medicines for future generations.

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Raw nerve: Drugs may get costlier as prices of ingredients surge 30%

India's medicine prices are poised for a sharp increase due to a 30% surge in raw material costs, driven by container ship scarcity following the Iran war. This scarcity is hindering the movement of crucial ingredients from China, impacting local manufacturing and potentially forcing producers to pass on higher expenses to consumers.

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India's exports of active pharma ingredients at Rs 41,500 cr surpassed imports in FY25

With API exports hitting an impressive Rs 41,500 crore last fiscal year, India has outperformed its imports of Rs 39,215 crore. The government is pushing for a self-reliant economy via the Production Linked Incentive scheme, strategically aimed at cutting down import connections, notably with China.

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Pharma exporters seek freight sops and logistical support as costs rise

As tensions in West Asia escalate, Indian pharmaceutical exporters are grappling with surging costs. In response, Pharmexcil is advocating for government interventions, including freight subsidies and enhanced logistical support. Meanwhile, companies are pivoting towards alternative shipping routes and ramping up their buffer stocks in anticipation of potential disruptions.

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Looking beyond seasonal sniffles: Protecting children's immunity from climate instability

Climate change is disrupting traditional illness patterns, affecting children's health. Savlon Swasth India Mission promotes proactive hygiene with the S.H.A.K.E. formula. This strategy encourages sanitizing, handwashing, doctor consultations, wound care, and nutritious meals. These habits build resilience against unexpected illnesses. The mission has positively impacted millions of children through hygiene education programs.

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Cipla USA recalls Nilotinib anti-cancer capsules over manufacturing issue: USFDA

Cipla USA is recalling over 400 cartons of its generic anti-cancer drug Nilotinib Capsules (150 mg and 200 mg) due to a manufacturing issue, the US Food and Drug Administration has said. The recall affects specific batches distributed in the United States.

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HLL Lifecare to expand AMRIT Pharmacies to 550 outlets by 2027

HLL Lifecare will significantly expand its AMRIT pharmacy network across India. The number of outlets will more than double to over 550 by December 2027. This initiative aims to make life-saving medicines and implants more affordable and accessible. Special focus will be on underserved and remote regions. The expansion involves an investment of Rs 100 crore.

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India set to lead global homoeopathy with certified quality frameworks: Experts

India is set to lead the global homoeopathy market. Strong clinical expertise and practitioner networks are driving this growth. Internationally recognised quality certifications like AYUSH Premium Mark and NABL accreditation are key. Indian brands are now well-positioned to challenge established European dominance. This marks a significant shift in the global homoeopathy landscape.

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Middle East conflict hits medical tourism, Indian hospitals tap other markets

Indian hospitals are diversifying patient sources to Southeast Asia, Africa, and Central Asia as the Middle East conflict disrupts medical travel. This shift aims to mitigate revenue losses from the region, which contributes significantly to their medical value travel earnings. Hospitals are also enhancing teleconsultation services and seeking government support for direct flights to maintain patient inflows.

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Cipla recalls over 400 cartons of cancer drug in US: FDA

Cipla USA is recalling over 400 cartons of its anti-cancer drug Nilotinib Capsules. The recall is due to a manufacturing issue where the capsules failed to meet specifications. This is a voluntary Class III recall, meaning it is not expected to cause adverse health consequences.

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FDA official overseeing vaccines resigns amidst controversy

A key US Food and Drug Administration official responsible for vaccines is departing at the end of April. Vinay Prasad faced criticism for health policy decisions, particularly concerning Covid-19 vaccine efficacy. His exit follows controversies, including refusing to review a flu vaccine application. Prasad had previously raised doubts about Covid-19 vaccine safety.

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Key drug prices may surge on hoarding and higher demand

Escalating Middle East conflict is expected to increase demand for essential medicines. This surge could lead to higher drug prices, potentially benefiting Indian pharmaceutical manufacturers. Companies are monitoring the situation closely. Increased demand for chronic and acute therapy drugs is anticipated. Indian firms may see export disruptions but also higher overall demand if the conflict extends.

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Obesity & diabetes are world's next health "tsunami", warns ebola discoverer Peter Piot

A leading virologist warns of a global tsunami of obesity and diabetes, surpassing viral threats. India faces significant vulnerability as diabetes rates surge. While pandemic preparedness has improved technically, societal trust remains a challenge. Innovations like new anti-obesity drugs offer hope but require broader access and lifestyle changes. India should prioritize discovery and innovation in biopharma.

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Pharma exports may take up to $500 million hit as freight costs rise

India's drug exports face a significant threat from the Iran war. Higher freight costs and shipping companies avoiding Gulf routes could impact shipments worth $300-500 million. This disruption affects both raw material imports from China and finished product exports to West Asia and beyond. Companies are building inventories to manage potential delays.

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India & China must-win markets on rising middle-class households: Reckitt Chief

Reckitt Benckiser sees India and China as vital growth markets. The company's CEO highlighted the expanding middle class in these nations. Emerging markets are driving Reckitt's revenue expansion. India and China showed strong growth in the last quarter. This performance helped offset weaker results in developed markets. Reckitt aims to increase its reach in India through improved distribution.

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Iran war could disrupt India’s pharma exports by up to $500 million

The Iran war is impacting India's drug exports. Higher freight costs and shipping refusals to Gulf hubs are causing concern. Industry estimates suggest a potential loss of $300-$500 million. While manufacturing remains unaffected, logistics are complicated. Companies are maintaining inventories to ensure supply continuity. The situation could lead to temporary supply challenges.

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India pharma exports risk disruption if Middle East conflict widens

Indian drug exports face significant challenges. A wider Middle East conflict could disrupt vital shipping routes. This may lead to longer transit times for temperature-sensitive medicines. Increased freight costs and potential delays in key markets like the UAE and Saudi Arabia are also concerns. Air cargo routes are also at risk.

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Urban India faces metabolic health crisis as 73 million are overweight or obese

In India's vibrant urban landscape, obesity and diabetes are becoming formidable adversaries. A new analysis highlights that while countless individuals are caught in the grip of these health challenges, there's a startling lack of awareness about innovative GLP-1 weight loss medications. Interestingly, informed individuals express considerable eagerness to explore these options.

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Ahead of its time, a GLP-1 drug almost made it out of India

Fifteen years back, Zydus Lifesciences introduced ZYOG1, an oral GLP-1 agonist that sparked excitement for its implications in diabetes management and weight loss. Unfortunately, due to prohibitive clinical trial costs and a skeptical outlook on the obesity market, Zydus chose to shelve further development.

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Child hears again 18 months after brain stem implant at AIIMS

A young boy in India has received a groundbreaking auditory brain stem implant. This marks a first for AIIMS. The surgery was performed after conventional implants were not suitable. The child is now responding to sounds and speaking more clearly. Doctors highlight the importance of early detection for hearing loss.

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NATCO Pharma launches generic blood cancer treatment medicine in US

NATCO Pharma has launched generic Pomalidomide capsules in the US. This drug treats blood and bone marrow cancer. It is a generic version of Celgene's Pomalyst. The launch is in partnership with Breckenridge Pharmaceutical. This move aims to make specialty medicines accessible. It offers an affordable solution for patients.

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Eli Lilly sticks to premium pricing for its innovator drug ahead of generics wave

Eli Lilly remains optimistic about strong demand for its weight-loss and anti-diabetes injectable, tirzepatide (sold as Mounjaro), despite its premium pricing, even as lower-cost semaglutide generics prepare to enter the Indian market.Winselow Tucker, president and general manager of Eli Lilly and Company (India), told ET that the company sees room for both branded innovator drugs and generics to thrive simultaneously in the rapidly expanding domestic segment.

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All our AI models have scientists in loop, says MSD chief AI officer

MSD's Chief AI Officer, Anton Groom, highlights AI's transformative role in drug discovery. AI models like TEDDY and KERMT are assisting scientists, identifying new drug targets and refining lead identification. This technology is accelerating the development of new medicines, with two AI-discovered molecules already in clinical trials.

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Brain can keep producing new neurons in old age, but Alzheimer’s may disrupt the process: Study

New research reveals the adult brain generates fresh nerve cells in the hippocampus, vital for memory. This ability declines in Alzheimer's patients. Scientists observed this process in postmortem brain samples. Healthy older adults show continued neuron production.

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ACC clears Dr Rajeev Singh Raghuvanshi’s reappointment as Drugs Controller (India)

Dr Rajeev Singh Raghuvanshi will continue as Drugs Controller (India) at CDSCO. His reappointment is on a contract basis for one year starting March 1, 2026. This decision follows a proposal from the Department of Health and Family Welfare. Dr Raghuvanshi heads the CDSCO, responsible for drug quality and new drug approvals.

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Zydus Lifesciences gets USFDA nod to market generic drugs

Zydus Lifesciences has won regulatory clearance in the United States to launch generic Ivermectin and Dapsone tablets. Used to treat parasitic worm infections and leprosy, the approval signals progress in the company's US growth strategy and broadens its market footprint.

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Abbott signs pact with Novo Nordisk to offer semaglutide

Semaglutide, sold by Novo Nordisk under brands such as Ozempic and Wegovy, goes off patent on March 21 in India. A raft of Indian generic drug makers has already lined up the launch of their generic semaglutide drugs immediately after the patent expiry, prompting the company to brace up for the upcoming competition in the GLP-1 market.

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Lupin receives USFDA EIR for Goa facility with VAI status

Drug maker Lupin said it has received an Establishment Inspection Report from the US Food and Drug Administration for its Goa-based manufacturing facility, with a Voluntary Action Indicated classification following a November 2025 inspection.

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India moves closer to dengue vaccine as final trials underway

An Indian vaccine candidate, DengiAll, is in its final testing phase. This single-dose shot offers hope against the deadly dengue disease. Over 10,000 volunteers are participating in the trials. If successful, DengiAll could be available next year. This development is crucial for India and other lower-middle-income countries facing rising dengue cases.

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Dräger India collaborates with Breach Candy Hospital to advance clinical education

Dräger India and Breach Candy Hospital have partnered to enhance clinical education and skill development for healthcare professionals. This collaboration brings the Dräger Medical Academy to Mumbai, offering digital learning modules and VR-based simulation training to bridge skill gaps and improve patient safety. The initiative aims to foster continuous learning and readiness in India's evolving healthcare landscape.

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Navigating environmental shifts: How proactive hygiene shapes a child's future

In today's unpredictable climate, raising children requires a proactive approach to health beyond traditional methods. Savlon Swasth India Mission's podcast, The Doc's Pod, emphasizes science-backed hygiene practices as a strategic tool for physical empowerment. By integrating habits like regular handwashing and surface sanitization, families can build a robust foundation for enduring health and cognitive development.

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Alembic Pharma gets USFDA nod for generic drug

Alembic Pharmaceuticals has secured approval from the US health regulator for a generic seizure medication. The company received final clearance from the USFDA for Lamotrigine orally disintegrating tablets. This drug is therapeutically equivalent to GlaxoSmithKline's Lamictal. It is used for various seizure types in patients aged two and older. The market for this medication is estimated at USD 27 million.

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Zydus plans launch of semaglutide generic in reusable pen form

Zydus Lifesciences is set to launch a generic version of the weight-loss injection semaglutide next month. The drug will be available under brand names Semaglyn, Mashema, and Altreme. Zydus will offer a unique reusable pen for easier dosage adjustment. This move aims to simplify treatment for patients managing Type 2 diabetes and obesity.

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GST department initiates inspection and search ops at Lupin's office

Maharashtra's Goods & Services Tax Department has initiated inspection and search proceedings at Lupin's registered office. The pharmaceutical giant stated that these actions will not impact its financials, operations, or other activities. Lupin recently reported strong Q3 FY26 growth, with highest-ever US sales and double-digit growth in India.

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India’s weight-loss drugs to get cheaper as semaglutide patent expires

Affordable generic versions of popular weight-loss drugs Wegovy and Ozempic are set to launch in India. This follows the patent expiry of semaglutide, the key ingredient. Several Indian pharmaceutical companies are preparing for a March 21 launch.

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Dr Reddy's gearing up for March debut of generic semaglutide Obeda, sources say

Dr Reddy's Laboratories is poised to launch its generic semaglutide injection, potentially named Obeda, in India by March. This move anticipates the March 2026 patent expiry for the active ingredient in Novo Nordisk's Ozempic and Wegovy. The Indian drugmaker plans competitive pricing, aiming to capture a significant share of the growing diabetes and obesity market.

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Merck & Co to create a separate cancer unit as patent cliff looms

Merck & Co is restructuring by splitting its drug division into two separate businesses. The change is designed to spotlight its fastest-growing medicines as the blockbuster cancer therapy Keytruda nears patent expiration. The company plans to emphasize newer products, including a pneumonia vaccine and a treatment for lung disease, as key drivers of its next growth phase.

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Drug regulator cracks down hard on non-compliant cough syrup makers

Authorities are cracking down on hundreds of cough syrup manufacturers failing quality checks. This action follows tragic deaths linked to toxic ingredients. Inspections are ongoing, with strict measures like unit closures and license cancellations being implemented. The drug regulator aims to eliminate substandard cough syrup production. Manufacturers must adhere to new quality standards or face closure.

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Government urges pharma sector to anchor global supply chains via quality, innovation

Union Minister J P Nadda urged India's pharmaceutical industry to lead global supply chains with quality and innovation. India is embracing new technologies for disease detection and diagnostics. Initiatives like Biopharma Shakti and PRIP are boosting manufacturing and research. The nation is committed to regulatory excellence and aligning with global standards. A quality-first approach is key to sustained global competitiveness.

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India's drug regulator inspected 90% of cough syrup makers, found lapses, official says

India’s pharmaceutical regulator has launched a thorough inspection of cough syrup manufacturers, discovering several discrepancies in their operating procedures. This decisive action follows alarming reports of child deaths linked to these syrups.

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Biosimilars & innovation are Dr. Reddy’s growth pill: Generics to remain core business, says co-Chairman & MD GV Prasad

Dr Reddy's Laboratories is strategically shifting focus towards biosimilars and innovation. The company is increasing investment in biosimilars, anticipating significant growth within five years. Generics and active pharmaceutical ingredients will continue to be major revenue sources. Dr Reddy's aims to compete in a biologics-led future by investing in research and development.

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Expects Pen-G production capacity to touch 10k metric tonnes in 12 months: Aurobindo Pharma

Aurobindo Pharma is set to boost Penicillin-G output to over 10,000 metric tonnes annually. Its China manufacturing facility is projected to reach EBITDA break-even this quarter. The company is also advancing its US operations and developing complex generics. These strategic moves aim for sustainable growth and improved profitability.

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BahiaFarma, Biocon, Bionovis inks MoU in pharma sector

India and Brazil signed multiple Memoranda of Understanding (MoUs) during Brazilian President Lula da Silva's visit. Key agreements include a pact for developing a breast cancer medicine, cooperation in iron ore blending at Gangavaram Port, and R&D in strategic pharmaceutical ingredients. ApexBrasil and FICCI also agreed to boost trade and investment.

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Quality Care India plans to invest Rs 600 crore to set up healthcare facility in Nagpur

Quality Care India Limited is set to invest Rs 600 crore in a new 350+ bed multi-speciality hospital in Nagpur. The facility, to be developed on Maha-Metro land near Kasturchand Park Metro Station, aims to strengthen healthcare infrastructure in Central India. This project, a public-private partnership, is expected to create over 1,500 jobs and enhance regional healthcare capacity.

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Novartis exits India arm, ChrysCapital-led group buys 70.68% stake for ₹1,446 crore

Swiss drugmaker Novartis AG is selling its 70.68% stake in its Indian unit for Rs 1,446 crore to a consortium led by ChrysCapital. This divestment aligns with Novartis' strategy to become a pure-play innovative medicines company, while it maintains a significant presence in India through its wholly owned subsidiary.

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Drugmakers flag concerns over blue-strip antibiotic labels

The government mandated a blue line on antibiotic packaging to curb misuse. However, pharmaceutical companies argue this will disrupt operations and finances. They believe the measure lacks scientific backing and global alignment. Industry associations are urging the government to withdraw the notification. Existing regulations already address antimicrobial resistance concerns.

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ChrysCapital, two others launch open offer for Novartis India

A consortium including WaveRise Investments, ChrysCapital, and Two Infinity Partners is set to acquire a significant stake in Novartis India. This move is part of Novartis's strategy to divest its stake. The transaction is expected to conclude in the third quarter of 2026. Novartis will continue its operations in India through Novartis Healthcare.

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Indian drugmaker Sai Life Sciences to boost headcount by about 20% amid global demand upswing

Sai Life Sciences will boost its workforce by over 700 employees next financial year. This expansion supports growing global demand for its services. The company is increasing capacity to meet this demand. New hires will focus on scientific, technical, and management roles. This move reflects a broader trend of global pharma companies expanding in India.

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Thyroid, antibiotic drugs face fresh safety warnings after national review

New safety warnings are coming for two common medicines, doxycycline and carbimazole. Indian drug regulators have identified potential mental health side effects for doxycycline. Carbimazole will now carry stronger warnings about a rare but serious blood disorder. Manufacturers must update prescribing information. These changes aim to improve patient safety by highlighting important risks.

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Zydus launches biosimilar for ophthalmic care

Zydus Lifesciences has introduced Anyra, its first indigenously developed biosimilar for the treatment of visual impairment in India. This innovative drug, akin to Aflibercept 2 mg, addresses vision loss resulting from diseases like diabetes.

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Pharma firms asked for side-effects of common medicines

India's drug regulator has issued new safety warnings for common medicines. Doxycycline, an antibiotic, will now list side effects like anxiety and dizziness. Carbimazole, used for thyroid issues, will highlight the risk of a life-threatening condition called agranulocytosis. Manufacturers must update package inserts and promotional materials. These changes follow recommendations from pharmacovigilance experts to ensure patient safety.

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Warburg Pincus talks in final lap to buy Integrace Health for Rs 1,200 crore

Integrace is currently owned by homegrown PE fund True North and Singapore sovereign investor Temasek Holdings. True North Fund VI LLP holds a 55.83% stake in Integrace, while Temasek arm V-Science Investments Pte owns 43.91%.

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Steroid abuse among gym-goers raises heart, liver risks; issue raised in Parliament

Young people are facing severe health issues due to steroids and unsafe supplements. Doctors report liver toxicity, infertility, and aggression. Heart specialists warn of life-threatening consequences like heart attacks. Mental health experts note links to depression and anxiety. The market for these substances requires stricter checks and greater awareness among youth.

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Seeing with sound: AIIMS distributes AI-powered smart glasses to help visually impaired

AIIMS has equipped 53 visually impaired individuals with advanced AI-powered smart vision glasses, transforming their environments into audible guidance. This innovative project empowers both children and adults to navigate life with newfound independence.

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AI can address health inequities, but cannot replace human touch: Union MoS Health Anupriya Patel

Speaking at the AI Impact Summit in the national capital, Patel asserted that India's governance model positions AI as an enabler and force multiplier, bringing the country closer to the goals of inclusivity and health equity.

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29 vitamin-mineral FDC drugs under review for possible ban over 'irrational' tag

A looming ban on twenty-nine vitamin and mineral combination drugs has sparked a heated debate. Initially flagged as irrational by an expert panel in 2015, these products are now being re-evaluated by a specialized sub-committee. Before any final ruling, the companies will be given a chance to defend their products.

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Lupin signs supply deal to launch antidepressant in Canada

Drug firm Lupin has partnered with Spektus Pharma. They will commercialise the antidepressant DeslaFlex in Canada. This collaboration combines Lupin's Canadian presence with Spektus's formulation expertise. It aims to offer patients more personalized care for Major Depressive Disorder. The deal strengthens Lupin's central nervous system portfolio. Lupin shares saw a slight increase on Monday.

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Alkem Labs' Chakan facility gets six observations in USFDA inspection, no data integrity issues

Alkem Laboratories announced its subsidiary Enzene Biosciences received a Form 483 from the USFDA. The inspection at the Chakan manufacturing unit resulted in six procedural observations. The company highlighted zero observations related to data integrity. Enzene is preparing its response to the USFDA within the given timeline. Corrective actions are also being initiated.

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Govt looks to provide access to AI resources to medical students: Official

The government plans to give medical students access to e-books and AI tools. This initiative will begin with 57 government medical colleges in smaller towns and rural areas. The aim is to improve students' skills by providing better access to digital and AI-powered learning materials. The program will gradually expand to include private colleges later.

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Adven Biotech says it's India's first homeopathic brand to get NABL certification

Adven Biotech achieves a significant milestone as India's first homeopathy brand to earn NABL certification. This accreditation underscores India's commitment to global healthcare standards in the Ayush sector. The certification validates Adven's quality control and testing laboratories, aligning with Prime Minister Modi's vision for Ayush. It aims to boost confidence and expand the global acceptance of Indian homeopathy.

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GST rejig marks key shift towards making cancer care affordable, AIIMS researchers says

AIIMS researchers highlight recent GST reforms, including tax exemptions on cancer drugs and medical equipment, aiming to make cancer care more affordable. Increased taxation on tobacco products is also noted as a positive step for public health and revenue generation for cancer initiatives.

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India becoming backbone of global clinical research

India has emerged as a key player in international clinical trials, showcasing resilience even in the face of global hurdles. With research and innovation on the rise, firms like Parexel recognize India's crucial contribution to ensuring consistent business operations. Instead of threats, artificial intelligence presents avenues for professionals to expand their roles and skillsets.

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Alkem Labs unit to buy up to 55% of Occlutech for $118 million

Alkem Laboratories is entering the advanced cardiovascular devices market. Its medical devices unit will acquire a significant stake in Switzerland's Occlutech Holding. This strategic move aims to access high-value global markets. The deal is expected to finalize by June 2026. Occlutech is a key player in Europe's minimally invasive cardiac implants.

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AIIMS Delhi first in country to announce launch of face transplant programme

AIIMS New Delhi has become the first hospital in India to introduce face transplantation, a complex reconstructive procedure for patients with severe facial deformities. The Department of Plastic, Reconstructive and Burns Surgery has begun creating a patient registry and is conducting specialised training, including a cadaveric workshop, with support from international expert Dr Indranil Sinha of Harvard Medical School.

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HUL turns ₹70 cr bet in Wellbeing Nutrition into ₹307 cr exit

Hindustan Unilever has divested its 19.8% stake in Wellbeing Nutrition to UVS Pharma for Rs 307 crore. This move comes after HUL's initial Rs 70 crore investment in 2022. The transaction, expected to conclude by March 2026, sees Wellbeing Nutrition valued at approximately Rs 1,600 crore.

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Zydus settles US Mirabegron patent dispute with Astellas for $120 million

Zydus Lifesciences and its US subsidiary have settled patent litigation with Astellas Pharma over Astellas' Myrbetriq. Zydus will pay Astellas $120 million upfront and a per-unit licensing fee on generic Mirabegron sales until September 2027. This agreement resolves all disputes and allows Zydus to continue marketing its generic version in the US.

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USV Pharma leads race to buy 85% stake in Wellbeing Nutrition at Rs 1,600 crore valuation

The Mumbai-based brand, owned by Nutritionlab, counts Hindustan Unilever and Fireside Ventures among its early backers. HUL and Fireside — holding 19.8% stake each — will exit with more than fourfold returns. Both invested in Wellbeing Nutrition about three years ago when the company was valued at about Rs 350 crore.

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Trial by fire: Novelis may see bigger cash flow hit

In the wake of a second devastating fire at its Oswego facility, Novelis Inc. has revised its expectations dramatically, now forecasting a staggering impact on its free cash flow. Originally bracing for a loss of $550-650 million, the company is now looking at potential damages between $1.3-1.6 billion prior to insurance compensation.

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Zydus Life cleared to sell life-saving cancer drug; SC tells Bristol Myers to map patents

The Supreme Court has provided Zydus Lifesciences with the go-ahead to launch its cancer drug biosimilar, countering efforts by Bristol Myers Squibb to halt its progress. The court has mandated that BMS verify how Zydus's product aligns with their patent claims, with options for BMS to request provisional support from the High Court following this analysis.

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Warburg-Mubadala leads race to buy majority in Soframycin maker

Exciting developments are afoot as Encube Ethicals, a key player in the pharma contract manufacturing sector, approaches a significant acquisition. The frontrunners, Warburg Pincus and Mubadala, are intensifying their bids, valuing the company at approximately ₹16,500 crore. This move underscores the burgeoning interest investors have in Indian CDMO companies, fueled by global supply chain shifts and evolving US policies.

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French pharma giant Servier to invest €15 million to launch global single-pill platform 'GATINN' in India

French pharma group Servier is expanding in India with a €15 million investment to launch GATINN, a global platform for single pill combinations (SPCs) targeting cardiometabolic and venous diseases. The India-based hub will coordinate research, manufacturing, and exports to international markets, aiming to improve patient adherence by combining multiple drugs into a single daily dose.

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IHH Healthcare, Fortis launch initiative to strengthen healthcare innovation ecosystem

IHH Healthcare, in partnership with Fortis Healthcare, is proud to introduce IHH Catalyst. This groundbreaking initiative is designed to fast-track the integration of innovative technology in healthcare across India. By empowering promising health-tech and med-tech startups to shift from concept to concrete implementation, IHH Catalyst aims to elevate patient care and optimize hospital processes.

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AstraZeneca gets CDSCO nod to market cancer drug Imfinzi for additional indication

AstraZeneca Pharma India has secured approval from India's drug regulator for Durvalumab, marketed as Imfinzi. This new indication allows its use in treating advanced or recurrent endometrial cancer. The drug will be administered in combination with other therapies for initial treatment. Following this, Durvalumab will be used as maintenance therapy for specific patients.

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Lupin clears Mirabegron patent dispute with Astellas in $90 million deal, secures US sales continuity

Drugmaker Lupin has settled a patent infringement dispute with Astellas Pharma over its Mirabegron product for $90 million. The agreement includes a $75 million prepaid option payment and a per-unit license fee. This resolution allows Lupin to continue marketing Mirabegron in the U.S., removing a significant legal obstacle.

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Decide on Piramal's Dahej plant in a week: Supreme Court to Gujarat Pollution Control Board

The Supreme Court has issued a swift order for the Gujarat Pollution Control Board to review Piramal Pharma's appeal to reactivate its Dahej manufacturing site, which was closed due to serious allegations related to hazardous waste management. The firm sought interim relief but was turned down by the court.

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Sampre Nutrition arm to set up facility in Egypt

Sampre Nutrition will expand its global reach with a new manufacturing unit in Egypt. Orascom Industrial Parks has approved land for food processing and confectionery. This facility will boost production and support international growth. The company recently partnered with Reliance Consumer Products. Sampre Nutrition saw a significant revenue increase in the first half of the year.

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Sun Pharma, Dr Reddy's & Lupin call for big push in drug innovation

Top Indian pharmaceutical leaders are urging a significant boost in research and development. They believe this focus on innovation is crucial for India to become a global biopharma manufacturing hub. Leaders from Sun Pharma, Cipla, Dr Reddy's Laboratories, and Lupin highlighted the need for greater investment and a shift towards developing novel drugs.

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India expected to see surge in Parkinson's disease, becoming 2nd-highest in 5 yrs: Experts at 6th International Annual Symposium-2026 in Kerala

India faces a surge in Parkinson's disease cases, potentially becoming second globally. Young-onset Parkinson's is a growing concern in Southeast Asia. Experts at a Kerala symposium highlighted the need for region-specific research and affordable treatments. Local manufacturing and international collaboration are key to expanding access to care for millions of patients.

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Sun Pharma to stay disciplined on M&A, says Dilip Shanghvi

Sun Pharma plans a careful acquisition strategy. The company prioritizes organic growth to remain an attractive investment. Chairman Dilip Shanghvi highlighted a focus on innovative medicines in the US. Smaller acquisitions are being considered for emerging markets. The firm is also evaluating the biosimilar sector. This approach aims to strengthen long-term capabilities.

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Battle for cooking oil: Nutritionists reveal which oil is best and what separates one from another

The battle for cooking oil has been heating up — with everything from coconut, mustard and refined oils fighting for shelf space, while avocado oil puts in an appearance now. ET asks experts whether any one oil can ever triumph over others.

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Strengthening the India-US medicines partnership important: IPA

The Indian Pharmaceutical Alliance welcomed an interim trade agreement between India and the US, emphasizing that medicine security is crucial for national security. The pact aims to boost bilateral trade by reducing import duties on various goods, including generics, and offers Indian MedTech exporters a competitive edge in the US market.

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Wipro seeks Schedule M exemption for Tumkur plant, regulator to review plea

Wipro has sought relaxation in requirement of Schedule M for specific categories like disinfectants. The product, Maxkleen, has been registered as a drug. The company has asked to allow them to manufacture the product without a drug licence.

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Shukra Pharma gets YEIDA LoI for Rs 600-crore facility

Shukra Pharmaceuticals will establish a Rs 600-crore facility in Greater Noida. This plant will produce advanced surgical robotics and BNCT technology. The project aims to create over 900 direct jobs. A partnership with Borns Medical Robotics Inc. will bring surgical robotics to India. This venture seeks to make high-precision surgery affordable and accessible across India and Asia.

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Alembic Pharmaceuticals gets USFDA nod for generic Parkinson's disease treatment tablets

Alembic Pharmaceuticals has secured a significant approval from the US health regulator. The company's generic version of Carbidopa, Levodopa, and Entacapone tablets, used for Parkinson's disease, has been cleared by the USFDA. This development marks a crucial step for Alembic in the US market.

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Drug regulator steps up oversight on product changes after approval

Drug makers now need government approval for any quality changes to medicines. This applies to alterations affecting a drug's identity, strength, quality, purity, or potency. The regulator is strengthening manufacturing standards through risk-based audits and more inspections. This ensures only safe and effective medicines reach consumers. Manufacturers must inform the drug regulator about changes in manufacturing, packaging, or shelf life.

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Sun Pharma to pump in Rs 500 cr in Assam manufacturing unit

Sun Pharmaceutical will invest Rs 500 crore to establish a new manufacturing plant in Assam. This significant project will create over 500 direct employment opportunities. The company plans to implement the investment in two phases. Discussions covered land, water, power, and skilled manpower. Sun Pharmaceutical will focus on sustainable manufacturing practices.

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Biopharma Shakti: India targets China dependence, patent cliff

India is launching a major initiative to boost its biopharmaceutical manufacturing. This plan aims to reduce reliance on China for crucial drug components. It also seeks to capitalize on upcoming patent expirations of major global drugs. India will focus on becoming a hub for biosimilars and emerging biologics. This strategy will strengthen the nation's pharmaceutical industry on the global stage.

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AstraZeneca gets CDSCO approval for Durvalumab in gastric cancer treatment

AstraZeneca Pharma India has secured approval for Durvalumab. This drug, combined with chemotherapy, will treat gastric and gastroesophageal junction cancer. The approval comes from the Central Drugs Standard Control Organisation. This new treatment offers a perioperative immunotherapy approach for adult patients. It aims to improve survival rates for those with resectable forms of the disease.

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Medical gear firms told to 'promptly' flag adverse cases

Indian medical device firms must now promptly report all adverse events, both serious and non-serious, to the government's Materiovigilance Programme. This directive aims to boost patient safety and address concerns over underreporting of issues linked to locally manufactured equipment. Timely reporting is crucial for identifying risks and implementing necessary safety measures.

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US tariff cut to 18% to boost India’s medical device exports

India's medical device exports to the US will surge following a tariff cut. This move makes Indian products more competitive against China. Lower import duties will also benefit India's healthcare system by reducing costs for high-value equipment. Industry leaders hail the deal as transformative, unlocking significant market potential and fostering investment.

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Budget relief on the label: Govt proposes to drop duty on rare disease drugs

The Indian budget proposes exempting seven rare disease drugs from import duties. This move aims to lower costs for expensive life-saving medicines. Patient groups welcome the relief for out-of-pocket expenses. However, some believe duty cuts alone will not make these drugs affordable for most Indians. The proposal also includes duty waivers on anti-cancer drugs.

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Lupin rolls out generic oncology drug in US market

Drug firm Lupin has launched a generic cancer treatment medication in the US. The company introduced Dasatinib Tablets in various strengths. This product is bioequivalent to Sprycel Tablets. It is indicated for adults with Philadelphia chromosome-positive chronic myeloid leukemia. The US market for Dasatinib Tablets had significant sales.

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Budget 2026 gives biologics & biosimilars a major policy boost

India is set to become a global biopharmaceutical manufacturing hub. Finance Minister Nirmala Sitharaman announced a dedicated ₹10,000 crore program over five years. This initiative focuses on biosimilars and biologics, crucial for treating non-communicable diseases. The move aims to boost manufacturing, regulation, and clinical trials, positioning India for future global competition.

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Union Budget 2026: Govt to overhaul drug regulator CDSCO, announces Rs 10,000 crore ‘Biopharma Shakti’ push

India Budget 2026: India's drug regulatory authority, CDSCO, will be strengthened to meet global standards and speed up approvals. A new initiative, Biopharma Shakti, with a Rs 10,000 crore outlay over five years, will boost domestic production of biologics and biosimilars. This strategy includes establishing 1,000 accredited clinical trial sites and upgrading NIPERs.

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Budget 2026: Sitharaman launches 'Biopharma Shakti' with a Rs 10,000-crore bet to heal India, power manufacturing

Union Budget 2026: With the announcement of the 'Biopharma Shakti' initiative, India is gearing up to take the world stage in biopharmaceutical manufacturing. Finance Minister Nirmala Sitharaman revealed plans to inject Rs 10,000 crore into this sector over the next five years. This initiative will significantly enhance domestic production of biologics and biosimilars.

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Sun Pharmaceutical to adopt a 'disciplined' approach to M&A: Dilip Shanghvi

Asked about the strategic priorities in the US, he added: "Not only the US, but we have interest in selling innovative medicines globally... for emerging markets we are looking at tuck-ins or smaller acquisitions which we can look at integrating with our existing business to get scale in the emerging markets." Shanghvi added.

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Indoco Remedies gets USFDA nod to sell generic epilepsy medicine

Indoco Remedies has secured approval from the US health regulator for its generic Lacosamide oral solution. This medication is used to treat epilepsy in adults and children. The approval allows Indoco Remedies to market the drug, which is a generic version of Vimpat Oral Solution. Manufacturing will take place at their Goa facility.

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Bristol Myers moves SC to stop Zydus from selling biosimilar cancer drug

US firm Bristol Myers Squibb is in the Supreme Court seeking to halt Zydus Lifesciences from manufacturing and selling a biosimilar cancer drug. The court will hear the appeal on February 4. BMS markets the drug nivolumab under brands Opdivo and Opdyta.

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Minimum import price set for Penicillin G, salts

The Indian government has imposed a minimum import price on crucial pharmaceutical ingredients like penicillin G, amoxicillin, and 6-APA. This move aims to counter cheap imports from China and support domestic producers. The price restrictions will be in effect for one year. This measure applies to imports for domestic consumption, ensuring a level playing field for local manufacturers.

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Eco Survey: Pharma focus turns to value, innovation over volumes

India's pharma sector is moving towards high-value products like complex generics and biosimilars. The medical devices industry is also growing, with exports reaching new heights. Advanced manufacturing technologies are key to this expansion. India is a major global supplier of vaccines and is increasingly producing sophisticated medical equipment. This marks a significant step in high-tech medical manufacturing.

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Reliance, Capri Global to acquire Mumbai’s SevenHills Hospital

Reliance Industries and Capri Global will acquire Mumbai’s 1,500-bed SevenHills Hospital, ending an eight-year impasse. The hospital will be converted into a not-for-profit entity, with funds infused via equity support.

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Drug misuse: Govt may curb 'Pregabalin' sales

The government is looking to control the sale of Pregabalin. This common medicine is being misused. The government wants to make sure it is only sold with a doctor's prescription. This move follows concerns raised by authorities. Pregabalin is used for pain and seizures. Stricter rules are being considered to prevent its misuse.

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S&P Global upgrades Biocon Biologics credit rating To 'BB+'

Biocon Biologics has received a credit rating upgrade from S&P Global Ratings. The company's long-term issuer credit rating is now 'BB+' with a stable outlook. This upgrade follows Biocon's simplification of its capital structure and reduction of debt. New product launches and industry trends are expected to support Biocon's earnings growth in the coming years.

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India-EU trade deal: A tonic for pharma companies

India and the EU are set to eliminate tariffs on pharmaceutical products, a move expected to significantly benefit India's pharma industry by reducing input costs and improving access to advanced medicines. Experts believe this will enhance trade and collaboration, strengthening India's position in the EU market.

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India's over-the-counter drugs market to hit Rs 98,000 crore by 2030: Report

An EY report estimated that India's OTC market, valued around Rs 47,000 crore in 2024, is projected to grow to Rs 98,000 crore around 13 per cent CAGR through 2030.

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India-EU FTA to strengthen position of Indian formulations, medicines in EU

A new India-EU free trade agreement promises to boost Indian pharmaceutical exports. Lower tariffs will make Indian medicines more competitive in Europe. This deal also aims to improve access to affordable, high-quality medicines for Indian patients. Experts anticipate significant price reductions for advanced therapies in the coming years. The agreement strengthens trade and collaboration between the two regions.

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PRISM-PCI Conclave 2026 in Vapi highlights India’s evolving approach to heart care

The PRISM-PCI Conclave 2026 highlighted India's significant advancements in cardiac care, showcasing its evolution from a consumer to a contributor in medical technology innovation. The event emphasized precision-driven strategies and the growing role of home-grown technologies in addressing complex cardiovascular diseases, improving patient outcomes globally.

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Cipla plans deeper push in domestic market and chronic therapies over next 2–3 years

Cipla's incoming MD and CEO-designate, Achin Gupta, outlined a two-to-three-year strategy focusing on deepening the domestic market presence and pursuing selective inorganic growth and innovation. The company aims to strengthen its respiratory leadership and achieve similar dominance in cardiometabolic diseases and obesity, with a near-term focus on the GLP-1 weight-loss segment through its partnership with Eli Lilly.

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China halts sale of Sun Pharma drug used to treat dementia

China's medicine regulator has halted the import, sale, and use of Sun Pharmaceutical Industries' dementia drug, rivastigmine hydrogen tartrate capsules. A recent inspection revealed production process shortcomings, including contamination prevention and quality management issues. This follows a 2024 warning letter from the U.S. FDA regarding similar manufacturing practice violations at the same Indian site.

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India’s 'Healthcare Budget' crossroads: Why the next leap is about design, not just spend

Union Budget 2026: India's healthcare system faces a structural shift from episodic care to lifelong management of chronic diseases. The Union Budget must move beyond incremental spending to architect a resilient system by addressing hospital capacity, insurance viability, human capital development, and digital health integration. A multi-year roadmap is crucial for long-term growth.

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Sun Pharma, Cipla recall products in US over manufacturing issues: USFDA

Sun Pharma and Cipla, two leading drug manufacturers from India, are taking precautionary measures by recalling products in the United States due to safety concerns. Sun Pharma's recall involves their generic skin condition treatments, identified to have impurity problems, while Cipla is addressing contamination in an injection linked to particulate matter. These recalls align with the oversight of the U.S.

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Pitiless Cut: Blood money for a broken hip

India's Supreme Court has ordered Johnson & Johnson to pay more compensation for faulty hip implants. This decision comes after a long legal battle for justice for patients. The court's ruling fixes culpability on the global company. However, the compensation awarded to Indian patients is significantly less than what was given in the US. Many patients continue to seek relief.

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Sun Pharma gets DCGI nod to launch generic semaglutide for weight management

Sun Pharma has gained the green light from the DCGI for its much-anticipated generic version of semaglutide injection, targeting chronic weight management under the name Noveltreat. With Novo Nordisk's patent expiration on the horizon, this initiative marks a pivotal moment in accessible healthcare.

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Sun Pharma gets DCGI nod for Wegovy-like weight loss drug, launch after Novo Nordisk's patent expiry

Sun Pharma has received DCGI approval to launch Noveltreat, a generic semaglutide injection for chronic weight management in India. This GLP-1 receptor agonist will be available after patent expiry, offering a crucial treatment option for India's growing obesity and diabetes burden. The approval follows successful Indian clinical trials.

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New drugs could reach market sooner as govt halves trial review timeline

The Indian government is shaking up the pharmaceutical sector by slashing the review period for manufacturing applications for new drugs to 45 days. Now, manufacturers can initiate clinical trials or bioequivalence studies with just a prior notification to the regulators, ditching the old requirement for express permission.

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Bastar's first super-specialty hospital opens

Bastar region will soon have its first super specialty hospital. Located in Jagdalpur, the facility opens in February. Hyderabad-based Continental Hospitals partners with the Chhattisgarh government. This 240-bedded hospital will offer advanced medical services.

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Budget 2026: Industry leaders seek funding framework for innovation, R&D in pharma, MedTech

Industry leaders are calling for a structured funding framework in the upcoming Union Budget. This aims to boost innovation and R&D in India's pharmaceutical and MedTech sectors. The goal is to drive advanced research and achieve the Viksit Bharat vision. Companies seek support for complex therapies and improved patient access.

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Zydus launches biosimilar for treatment of multiple cancers

Zydus Lifesciences has launched Tishtha, the world's first biosimilar of Nivolumab, in India. This drug treats multiple cancers. Tishtha will be available in 100 mg and 40 mg dosages. The prices are significantly lower than the reference drug. This launch expands access to immuno-oncology therapies. The company aims to support patients with consistent care.

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Over 160 drug samples found sub-standard in December

A recent inspection by India's drug regulator has revealed a troubling statistic: 167 medication samples were classified as not of standard quality (NSQ) in December, with valuable insights from both central and state laboratories aiding the findings. Many of these samples consisted of widely used drugs, highlighting a critical need for heightened quality control.

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CDSCO finds over 160 drug samples as 'not of standard quality' for December

In December 2025, 74 drug samples were identified as Not of Standard Quality (NSQ) by Central Drugs Laboratories and 93 by State Drugs Testing Laboratories. Additionally, seven spurious drug samples were identified across various zones, manufactured by unauthorized entities. These findings are part of routine regulatory surveillance to ensure market safety.

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Drug maker Lupin inks licensing pact with Galenicum for injectable Semaglutide

Drug maker Lupin announced a significant partnership. Its subsidiary, Lupin Atlantis Holdings SA, has signed an agreement with Galenicum Health. This collaboration focuses on diabetes and weight management medication, specifically injectable Semaglutide. Galenicum will handle development and manufacturing. Lupin will manage regulatory submissions, approvals, and commercialisation.

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Delhi High Court denies interim protection to Alkem in 'A to Z' trademark case

The Delhi High Court has denied Alkem Laboratories interim protection in a trademark dispute. Prevego Healthcare & Research can continue selling its multivitamin product under the brand name Multivein AZ. Alkem Laboratories had claimed infringement of its A to Z and A to Z-NS trademarks. The court noted differences in fonts, color schemes, and trade dress.

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Novo Holdings buys 49% stake in Surya Hospitals

Novo Holdings, a major investment firm, has acquired a 49% stake in Surya Hospitals for an estimated Rs 1,000-1,200 crore. This strategic move highlights Novo Holdings' focus on specialized healthcare in India, particularly in women's and children's care, where Surya Hospitals has a strong reputation. The deal underscores the ongoing investment trend in the Indian hospital sector.

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Sun Pharma places non-binding offer for US-based Organon in its boldest global bet ever

Sun Pharmaceutical Industries Ltd has submitted a non-binding offer to acquire US-based Organon for an all-cash deal, securing $10-14 billion in acquisition financing. This move marks Sun Pharma's boldest global bet, aiming to bolster its presence in women's health biopharma and biosimilars. The acquisition, if successful, would be the largest by an Indian pharmaceutical company.

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Syngene expands research collaboration with Bristol Myers Squibb

Syngene International has extended its research partnership with Bristol Myers Squibb until 2035. This expanded agreement covers more services for drug development, from discovery to manufacturing. The collaboration, which began in 1998, will now focus on building new capabilities for future programs. This move aims to accelerate the delivery of new medicines to patients worldwide.

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Sun Pharma clarifies $10 bn Organon acquisition report, calls it 'speculative in nature'

Sun Pharma has addressed speculation regarding a potential $10 billion acquisition of US firm Organon. The Indian drugmaker stated the reports are speculative and no material event requires disclosure. Sun Pharma adheres to high governance standards. Organon, focused on women's health and biosimilars, was spun off from Merck in 2021.

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Sun Pharma looks to rise in US with $10 billion Organon buy

India's largest drugmaker, Sun Pharma, is considering a major acquisition. The company is evaluating the purchase of US-based Organon, a specialist in women's health. This potential deal is valued at around $10 billion. A successful acquisition would be a significant move for Sun Pharma, strengthening its presence in the US market.

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Brazil, Nigeria emerging as key export destinations for Indian pharmaceuticals

Indian pharmaceutical exports are seeing strong growth. Brazil and Nigeria are now important markets for Indian medicines. This shows a wider reach for Indian pharma products. The US remains the biggest buyer. Other countries like France and Germany are also increasing their purchases. This diversification strengthens India's position as a global medicine supplier.

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PE backed ASG Eye hires Morgan Stanley and three other bankers for upcoming IPO

ASG Hospital, a major eye care chain, is preparing for its initial public offering. The company has selected four investment banks to manage the process. ASG plans to raise between ₹3,000 and ₹4,000 crore. This offering is expected to take place in the financial year 2027. The move follows strong market interest in the healthcare sector.

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IHCL to aquire 51% stake in Brij Hospitality

Indian Hotels Company, backed by Tata Group, is acquiring a majority stake in Brij Hospitality. This move aims to bolster IHCL's presence in the boutique luxury hotel market. The deal, valued at up to Rs 225 crore, will integrate Brij's portfolio of 22 hotels. This acquisition is expected to be completed by March 2026.

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Zydus Lifesciences gets USFDA nod for generic blood disorder drug

Zydus Lifesciences has secured final approval from the USFDA for its generic Eltrombopag tablets. These tablets treat low platelet counts in specific blood disorders. The approval covers multiple strengths. Production will occur at the company's Ahmedabad facility. This development marks a significant step for Zydus in the US market.

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Delhi HC restores ban on 2 diabetes FDCs

The Delhi High Court has made waves with its recent judgment, reinstating a ban on two fixed-dose combination drugs for managing Type II Diabetes Mellitus, significantly affecting leading pharmaceutical corporations. The ruling reaffirmed the government's power to eliminate drugs deemed risky to health.

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Dr Reddy's launches generic OTC ophthalmic solution in US market

Dr Reddy's Laboratories has launched a new eye drop in the United States. This over-the-counter solution treats itchy eyes. It is an antihistamine eye drop. The company received approval from the US Food and Drug Administration. This launch expands their existing eye care products. It highlights their ability to bring store-brand equivalents to the US market.

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Indian hospital chain Narayana Health eyes international expansion

Narayana Hrudayalaya is gearing up to make its mark in Western healthcare markets. Leveraging its innovative, affordable healthcare model that has thrived in India, the company is now setting its sights on the UK as a strategic launchpad for further global expansion.

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Apollo Hospitals demerger is a biz call taken for shareholders, says Suneeta Reddy; rules out family rift

Apollo Hospitals MD Suneeta Reddy says the group’s restructuring is about business strategy, not family dynamics, aiming to unlock value by separating hospital and pharmacy-digital units. She stresses close ties with sister Shobana Kamineni, outlines expansion in metros and Tier-II cities, focus on preventive care, tech-led growth, and mentoring the next generation of leaders.

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Biocon arm gets USFDA nod for generic Everolimus tablets

Biocon's arm, Biocon Pharma Ltd, has secured USFDA approval for its generic Everolimus tablets. This medication aids in treating tuberous sclerosis complex, a rare genetic disorder causing tumors. The approval for 2mg, 3mg, and 5mg strengths bolsters Biocon's drug offerings, providing a new treatment option for adult and pediatric patients with specific TSC-related conditions.

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Alembic Pharmaceuticals gets USFDA tentative nod for generic cancer treatment drug

Alembic Pharmaceuticals has secured tentative approval from the USFDA for its Bosutinib tablets. These tablets are used to treat certain types of cancer, specifically chronic myelogenous leukemia. The approval covers the 400 mg strength. This development marks a significant step for Alembic in the US market. The company previously received final approval for other strengths of the same drug.

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Delhi HC clears Zydus to sell biosimilar of BMS cancer drug Nivolumab

The Delhi High Court has permitted Zydus Lifesciences to produce and market a biosimilar cancer drug. This decision comes as the patent for the original drug, Nivolumab, nears its expiration. The court prioritized patient access to affordable treatment. Zydus can now proceed with its biosimilar, ZRC-3276, while maintaining sales records.

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Budget 2026: Pharma, med-tech companies seek PLI extension to cover APIs

The industry expects the government to address these issues in the Union budget announcement this year. Sudarshan Jain, secretary general of Indian Pharmaceutical Alliance (IPA) said the recent global challenges like US tariffs, supply chain disruptions and geopolitical uncertainty have underscored the need for strategic support, and hence, restoring 200% weighted deduction for research and development expenditures would be a significant step.

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Aurobindo Pharma’s Dyrupeg faces Health Canada compliance notice

CuraTeQ Biologics, a part of Aurobindo Pharma, has secured a crucial approval from Health Canada for its biosimilar drug Dyrupeg. This medication helps cancer patients with low neutrophil counts. The approval confirms Dyrupeg's high similarity to an existing reference biologic drug. Earlier, Dyrupeg also gained marketing authorization in the European Union and the UK.

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Canadian pharmacy platform to offer India-sourced Ozempic to US patients

SaveRxCanada.to, an online pharmacy platform, announced it is now offering Ozempic sourced from India to U.S. patients at significantly lower prices than U.S. retail pharmacies. The company claims to connect patients with licensed international pharmacies, though Novo Nordisk denies any relationship with the platform.

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Cardiac drugs log highest sales in 2025 as NCD cases surge

Heart medicines led sales in 2025, a trend set to continue. Respiratory and anti-diabetes drugs followed. Cardiac drug sales grew 13%, with similar strong performance expected. Rising non-communicable diseases like hypertension fuel this growth. Increased awareness and longer treatment durations contribute.

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Ayushman Bharat: UP cuts claim pendency sharply, speeds up hospital payments

Uttar Pradesh is making waves in healthcare with significant advancements in settling Ayushman Yojana claims. The state is firmly committed to timely reimbursements for partner hospitals, leading to a culture of transparency in claims processing. These initiatives have slashed the backlog of pending claims, ensuring that hospitals provide swift treatment to Ayushman card holders.

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Granules India gets USFDA tentative nod for generic ADHD treatment tablets

Granules Pharmaceuticals, Inc., a subsidiary of Granules India, has achieved a significant milestone with the tentative green light from US health authorities for its generic amphetamine extended-release tablets, designed for managing attention deficit hyperactivity disorder.

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Future diabetes care seen leaning towards GLP-1 drugs

The diabetes treatment landscape in India is on the brink of transformation. Innovative GLP-1 medications are set to redefine therapy standards, providing remarkable advantages in glucose regulation and weight management, while also safeguarding vital organs such as the heart and kidneys.

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Budget 2026: Volume to value - How India can get a quiet superpower

India Budget: India's pharmaceutical industry, a global leader in volume, is poised to leverage its scale for greater international influence. The upcoming Union Budget 2026-27 presents a crucial opportunity to shift focus from low-margin generics to high-value segments like biologics and novel drug discovery.

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HC seeks Novo Nordisk's reply on Natco plea to revoke patent

The Delhi High Court has asked Novo Nordisk to explain why its patent for the diabetes and weight loss drug semaglutide should not be cancelled. Natco Pharma filed the petition. Novo Nordisk's patent expires in March. This has sparked patent disputes as other companies aim to produce their own versions of the drug.

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Biocon Biologics to introduce three new biosimilars for cancer treatment

Biocon Biologics will launch three new oncology biosimilars. These include Trastuzumab/Hyaluronidase, Nivolumab, and Pembrolizumab. The company aims to expand access to vital cancer treatments. These biosimilars will offer cost-effective alternatives. Biocon Biologics will have one of the most comprehensive oncology portfolios. This move strengthens its commitment to patient care.

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Max Healthcare partners with The Learning Lab for advance healthcare capacity building, research

Max Healthcare has partnered with UK-based The Learning Lab to advance healthcare capacity-building and foster joint research. The collaboration will co-create training modules for healthcare professionals, aiming to strengthen clinical competencies and improve patient outcomes. This initiative combines Max Healthcare's clinical experience with The Learning Lab's educational expertise to deliver practical, evidence-based learning.

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IIT Roorkee hosts 'AHEAD 2025' global health conference

IIT Roorkee hosted the "AHEAD 2025" International Conference on Health and Development, bringing together global experts to address critical challenges. The event focused on policy-relevant research for health systems resilience, climate health, and demographic change, aligning with India's development agenda and SDGs.

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Indian fertility experts advise caution on clinical use of new 'Non-Invasive' Embryo Genetic Test

Leading Indian fertility experts have cautioned against using non-invasive embryo genetic testing (niPGT) for routine clinical decisions. A joint review by ISAR, IFS, and ACE found the technique prone to high misdiagnosis rates, potentially leading to incorrect embryo selection or discarding. The technology, while promising, lacks sufficient evidence for clinical use.

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Budget for 'pharmacy of the world': What Sitharaman & Co can do to make medicines more affordable in India

Union Budget 2026: India's pharmaceutical landscape is on the brink of a transformative boom. To maintain this upward trajectory, the focus must shift towards fostering innovation and enhancing the efficiency of drug manufacturing. Strategic government funding is essential to bolster research initiatives, support production facilities, and strengthen healthcare frameworks.

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