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Alembic Pharmaceuticals receives EIR report from USFDA

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Capital Market

Following audit of its new injectable facility at Karakhadi

Alembic Pharmaceuticals has received Establishment Inspection Report (EIR) from US Food and Drug Administration (USFDA) for the inspection carried out by them at the company's New Injectable Facility (F-3) at Karakhadi during the period from 28 January 2021 to 5 February 2021, indicating that the USFDA finds the responses to their observations to be adequate. USFDA has also indicated that a compliance verification would be performed during re-inspection of the said Facility in the next review cycle.

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First Published: Oct 11 2021 | 3:05 PM IST

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