Entering the Indian medical device market presents a massive opportunity for manufacturers. However, navigating the approval process can be complex. This guide aims to a detailed understanding of the procedure involved in achieving medical device registration in India. A successful registration jour

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 provi