News Announcement

Cipla: USFDA Cgmp Inspection Completed At Cipla''s Manufacturing Facility In Goa

Pursuant to Regulation 30 of the SEBI (Listing Obligations and Disclosure Requirements) Regulations 2015 this is to inform you that the United States Food and Drug Administration (USFDA) conducted a cGMP inspection at our Goa manufacturing facility from September 16-27 2019.

The inspection ended with 12 observations none of which are related to data integrity. The Company will respond to the agency within the stipulated timeline.

Kindly take the above information on record.

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