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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