Entering the Indian medical device market presents a significant opportunity for companies. However, navigating the licensing process can be demanding. This guide provides a detailed understanding of the process involved in achieving medical device registration in India. A smooth registration journey starts with grasping the legal structure and key
Comprehensive Guide to Preparing A Plant Master File (PMF) For Medical Device Registration In India
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