Regulatory strategy & submissions with Central Drugs Standard Control Organization, Clinical Trial Design & Execution, Ethics & Regulatory Compliance, Drive Pre-CTA & CTA submissions, Prepare & review CTD modules, Design & execute clinical trials
Required Candidate profile
MSc in Cell & Gene Therapy, PhD
Exp in regulatory affairs and clinical development
Direct experience with CDSCO submissions & approvals
involvement in clinical trials for regenerative medicine
📌 Regulatory & Clinical Strategy Lead in Regenerative Medicine (Mumbai)
🏢 Rafaga Infoknowledge
📍 Mumbai
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