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USFDA conducts cGMP inspection at Cipla's Patalganga facility

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Issues 4 observations

Cipla announced that the United States Food and Drug Administration (USFDA) conducted a routine cGMP inspection for both Formulations and APIs at the company's manufacturing facility in Patalganga from 4 November 2019 to 13 November 2019.

The inspection ended with 4 observations, none of which were repeat or related to data integrity. The Company is committed to addressing these observations and will submit its response to the agency within the stipulated time

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(This story has not been edited by Business Standard staff and is auto-generated from a syndicated feed.)

First Published: Thu, November 14 2019. 16:05 IST