Cipla gets EIR from USFDA for Indore plant

23 Sep 2022 Evaluate

Cipla has received the Establishment Inspection Report (EIR) for its Indore plant, indicating closure of the inspection. The United States Food and Drug Administration (USFDA) had conducted product-specific pre-approval inspection (PAI) at the Indore plant on June 27 and July 1.

Cipla is a global pharmaceutical company which uses cutting edge technology and innovation to meet the everyday needs of all patients.

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