Entering the Indian medical device market presents a tremendous opportunity for businesses. However, navigating the approval process can be demanding. This guide seeks to a comprehensive understanding of the procedure involved in obtaining medical device registration in India. A efficient registration path starts with comprehending the legal struct

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