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  • Monitoring & ensuring implementation of current GMP & GLP norms in Manufacturing Unit of parenteral and solid oral dosage forms. Conducting internal audit as per USFDA, MHRA, TGA, MCC & WHO-GMP requirement Facing different regulatory audits (USFDA, MCC, WHO & MHRA) Preparing & implementing Quality Management System (QMS) Training, framing the documentation for all the departments (sops / protocols, and various other cGMP ...

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