Biocon gets EIR from USFDA for Biologics Drug Product facility in Bengaluru

05 Nov 2019 Evaluate

Biocon has received an Establishment Inspection Report (EIR) from the US Food and Drug Administration (USFDA) for its Biologics Drug Product facility in Bengaluru, stating the inspection is closed. This reaffirms Biocon Biologics' global scale manufacturing capability for high quality, affordable biosimilars for the US market.

The company had undergone a surveillance (routine) cGMP inspection of this Drug Product facility in Bengaluru from Aug 22 to Aug 30, 2019. The receipt of EIR indicates a successful closure of this inspection. The company is committed to highest standards of Quality and Compliance.

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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