Entering the Indian medical device market requires a thorough understanding of its stringent registration process. To ensure regulatory compliance and market access, manufacturers ought to navigate a multifaceted system. This involves submitting comprehensive applications to the Central Drugs Standa

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