USFDA completes inspection at Alembic Pharmaceuticals’ Oral Solid Formulation Facility

26 Jul 2024 Evaluate

United States Food and Drug Administration (USFDA) has completed GMP inspection at Alembic Pharmaceuticals’ Oral Solid Formulation Facility (F-I) located at Panelav. This was successfully completed without any Form 483 observation. The inspection was conducted from July 17, 2024 to July 26, 2024.

Alembic Pharmaceuticals, a vertically integrated research and development pharmaceutical company, has been at the forefront of Healthcare since 1907.


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