USFDA completes GMP, Pre-Approval Inspection at Dr. Reddy's R&D centre in Hyderabad

09 Dec 2023 Evaluate

United States Food & Drug Administration (USFDA) has completed a GMP and Pre-Approval Inspection (PAI) at Dr. Reddy's Laboratories’ R&D centre (Integrated Product Development Organisation or IPDO) in Bachupally, Hyderabad. The inspection was conducted from December 4, 2023 to December 8, 2023. The company has been issued a Form 483 with three observations, which it will address within the stipulated timeline.

Dr. Reddy's Laboratories is a multinational pharmaceutical company based in Hyderabad, Telangana in India. It manufactures and markets a wide range of pharmaceuticals in India and overseas.


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