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Alembic Pharma gets USFDA EIR for Jarod facility
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Vadodara: Alembic Pharma has announced that the Company has received an Establishment Inspection Report (EIR) with classification as "Voluntary Action Indicated (VAI)" from the US Food and Drug Administration (USFDA) for the inspection carried out at the Company's Solid Oral Formulation Facility (F-4) at Jarod, Vadodara.
The inspection was conducted from 14th November, 2024 to 22nd November, 2024.
Read also: Alembic Pharma bags USFDA final approval for schizophrenia drug Brexpiprazole
Alembic Pharmaceuticals Limited, a vertically integrated research and development pharmaceutical company. Headquartered in India, Alembic is a publicly listed company that manufactures and markets generic pharmaceutical products all over the world. Alembic's state of the art research and manufacturing facilities are approved by regulatory authorities of many developed countries including the USFDA.
Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751
Dr Kamal Kant Kohli-MBBS, DTCD- a chest specialist with more than 30 years of practice and a flair for writing clinical articles, Dr Kamal Kant Kohli joined Medical Dialogues as a Chief Editor of Medical News. Besides writing articles, as an editor, he proofreads and verifies all the medical content published on Medical Dialogues including those coming from journals, studies,medical conferences,guidelines etc. Email: drkohli@medicaldialogues.in. Contact no. 011-43720751