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Advanced course in GLOBAL REGULATORY AFFAIRS [GRA-API, Formulations, Medical Devices, Biosimilars, OTC]
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Advanced course in NUTRACEUTICALS[NUTRA]
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GLOBAL Medical Devices Regulations i.e. MDR course[India, Europe, USA, ASEAN, ROW markets]
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Computer System Validation, 21 CFR part 11, GAMP 5
Internal Auditor/Lead Auditor QMS 13485-2016, ISO 19011-2018 Course
Medical Device -Indian Regulation, BIS Submission, Sugam Portal Submission
Medical Device-European MDR, CE Mark
Medical Device- USFDA Submission
MDD to MDR Implementation
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