VENTURING INTO CDSCO MEDICAL DEVICE REGISTRATION: A COMPREHENSIVE GUIDE

The process of registering a medical device with the Central Drugs Standard Control Organisation (CDSCO) can seem complex. However, with a thorough approach and understanding of the requirements, you can effectively navigate this process. This resource aims to furnish you with the essential information to facilitate a successful registration experi

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