Natco Pharma gets EIR from USFDA for Telangana facility

​​The United States Food and Drug Administration (USFDA) had conducted pre-approval inspection at the company's drug formulations facility in Kothur village during the period from March 2 to 6, 2020, Natco Pharma said in a filing to the BSE.

from Healthcare/Biotech-Industry-Economic Times https://ift.tt/2S4lVI4
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