EXPLORING MEDICAL DEVICE REGISTRATION IN INDIA: A COMPREHENSIVE GUIDE

Entering the Indian medical device market presents a significant opportunity for manufacturers. However, navigating the approval process can be demanding. This guide provides a thorough understanding of the requirements involved in achieving medical device registration in India. A efficient registration path starts with comprehending the legal syst

In India, the Central Drugs Standard Control Organization (CDSCO) regulates medical devices in accordance with the Medical Device Rules 2017 India. For medical device registration India on the Sugam portal, one essential requirement is the submission of a Plant Master File (PMF). This document provides detailed information about the legal manufactu