Indoco’s Clinical Research Organisation receives zero 483s from US FDA

Indoco Remedies Ltd. announced today, that its Clinical Research Organisation, AnaCipher, located at Hyderabad successfully cleared US FDA Inspection

Indoco Remedies Ltd. announced today, that its Clinical Research Organisation, AnaCipher, located at Hyderabad successfully cleared the United States Food and Drug Administration (USFDA) inspection with zero 483s. The inspection was held from 14th October to 18th October, 2019. Commenting on this development, Ms. Aditi Kare Panandikar, Managing Director, Indoco Remedies Limited said, “This achievement is for the fifth time in a row and confirms the capabilities of our team at the CRO for maintaining highest quality standards and excellence in servicing our clients”. The CRO - AnaCipher conducts Bio-Equivalence and Bio-Availability (BA/BE) studies at its facility in Hyderabad and is spread over an area of 30,000 sq. ft. with 98 beds.

Tags : #Indoco #FDA #Inspection

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