Sai Life Sciences gets inspection certificate from PMDA for Bidar facility
Hyderabad: Sai Life Sciences, a global Contract Research, Development & Manufacturing Organization (CRO/ CDMO), has recently announced that the Japanese regulatory agency, Pharmaceuticals and Medical Devices Agency (PMDA) has completed a paper-based compliance inspection of its intermediate & API manufacturing facility in Bidar, India and issued a Certificate of...
Hyderabad: Sai Life Sciences, a global Contract Research, Development & Manufacturing Organization (CRO/ CDMO), has recently announced that the Japanese regulatory agency, Pharmaceuticals and Medical Devices Agency (PMDA) has completed a paper-based compliance inspection of its intermediate & API manufacturing facility in Bidar, India and issued a Certificate of Inspection.
Previously, the agency had conducted a three-day long physical audit in the year 2016 and had issued a Certificate of Inspection.
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