Sai Life Sciences gets inspection certificate from PMDA for Bidar facility
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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.
Making the announcement, Krishna Kanumuri, CEO & Managing Director, said, "We are delighted to receive a formal Certificate of Inspection from PMDA, Japan. We have been a reliable supplier of pharmaceutical API to the Japanese market for over five years and this certification is a reaffirmation of our commitment to fulfil the most stringent quality standards of the regulatory agency."
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