The Indian medical device sector is experiencing a period of expansion, presenting both possibilities for domestic and international players. To successfully operate within this evolving landscape, it is essential to have a clear understanding of the governing framework that oversees medical device

Entering the Indian market for medical devices presents a unique opportunity for manufacturers. To successfully distribute in this growing sector, it's crucial to understand the regulatory framework set by the Central Drugs Standard Control Organization (CDSCO). The CDSCO registration process can se

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