Regulatory Affairs Associate

By newrsi / November 8, 2024

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Regulation of Software as a Medical Device (SaMD) in India: A Beginner’s Guide
Understanding Accessories to Medical Devices in India
IVDs Registration in India
A Step-by-Step Guide to EPR Registration (Plastics, E-Waste, Batteries) in India
Labeling Requirements for Medical Devices (wrt MDR 2017 & amendments thereof)

We offer turnkey Regulatory Services, for India market, helping clients obtain import license and post approval registration support for Medical Devices, IVD & Cosmetics.

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