Entering the Indian medical device market presents a significant opportunity for manufacturers. However, navigating the registration process can be demanding. This guide provides a comprehensive understanding of the process involved in securing medical device registration in India. A smooth registration path starts with understanding the legal stru

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