Biocon receives EIR from USFDA for aseptic drug product facility

20 Nov 2017 Evaluate

Biocon has received Establishment Inspection Report (EIR) from US Food and Drug Administration (USFDA) in relation to the cGMP (current Good Manufacturing Practice) inspection of its aseptic drug product facility that was audited between May 25, 2017 to June 3, 2017. The USFDA has classified the outcome of this inspection as VAI (voluntary action indicated) and the EIR states that the inspection is closed.

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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