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Deepika Tak


pharmaceutical
West Blocton Health Center
India

Biography

 I have about 2 years of experience in Regulatory affairs. I had perceived M. Pharm. (Pharmaceutics) from Guru Jambheshwar University, Hisar (Haryana). Currently working as Executive DRA with Brawn Laboratories Limited, Faridabad. My work experience is in preparation & Compilation of Dossiers for Regulatory, Semi-regulatory & Non-regulatory Countries in formats like CTD, ACTD & Countries specific guidelines to fulfill regulatory requirement, Application of COPP. Prepare protocols & reports of Process Validation, Cleaning Validation, Equipment Qualification, Hold Time Study, Preparation of BMR & BPR, Preparation of SOP’s, STS-STP, Stability Study Data. Review of Finished Products COA’s. Handling of Query related to dossier either it is Manufacturing & Analytical, handling of market complaint.

Research Interest

  Regulatory affairs  

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