Feb
07
Alembic Pharma gets five observations from USFDA for Gujarat facility
Posted by
www.biotecnika.org
As per the USFDA, a Form 483 is issued to a firm's management at the
conclusion of an inspection when an investigator has observed any
conditions that in its judgment may constitute violations of the Food
Drug and Cosmetic (FD&C) Act and related Acts.
https://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/alembic-pharma-gets-five-observations-from-usfda-for-gujarat-facility/articleshow/80745383.cms
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May 11, 2025 at 8:28 PM
Ever wondered what a Form 483 from the FDA is? From my experience, it's basically a list of concerns observed during an inspection, highlighting potential compliance issues with regulations. It's definitely a document companies want to avoid! Speaking of avoiding problems, did you know Google celebrated pacman 30th anniversary with a playable doodle?
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