Glenmark Pharma gets 5 USFDA observations for Goa facility
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Mumbai: Drugmaker, Glenmark Pharma, has recently announced that the US Food and Drug Administration (USFDA) has issued Form 483 with five observations after an inspection at the Company's formulation manufacturing facility based out of Goa, India.
The inspection was conducted between May 12, 2022 and May 20, 2022.
"This is to inform you that the U.S. FDA has issued Form 483 with five observations after an inspection at the Company's formulation manufacturing facility based out of Goa, India between May 12, 2022 and May 20, 2022," the company stated in a BSE filing.
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