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USFDA completes inspection at Biocon’s arm’s Oral Solid Dosage manufacturing facility

20 Jan 2020 Evaluate

US Food and Drug Administration (USFDA) has completed Pre-Approval inspection at Biocon’s subsidiary -- Biocon Pharma’s Oral Solid Dosage manufacturing facility with Zero Observations. The inspection of the Bengaluru facility, which took place between January 13 and January 17, 2020, concluded with zero observations and no Form 483 was issued.

Biocon is India’s largest and Asia’s leading Biotechnology Company with a strategic focus on biopharmaceuticals and research services. It is a fully integrated, innovation-driven biopharma enterprise offering affordable solutions for chronic diseases to patient's worldwide.

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