GRP Regulatory Affairs Presentations
GRP's team of local experts have produced regulatory affairs related presentations to support Medical Device, Pharmaceutical, Cosmetic, Food Supplement Registration in the following countries. Included are Quality and Pharmacovigilance Presentations to answer some of the most asked topics associated to pre and post market activities such a pre-consultation meeting with Health Authority (ies), Price-reimbursement and lab testing.
USFDA Presentations
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China (NMPA) presentations
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Japan (PMDA) presentations
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South Korea (MFDS) Presentations
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Brazil (Anvisa) Presentations
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mexico (cofepris) presentations
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