Medical device import registration in the Indian market can be a complex process. Manufacturers seeking to introduce their products into the country must adhere to stringent requirements. A successful import process often involves careful planning and engagement with relevant authorities. Essential

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

The adventure of registering a medical device with the Central Drugs Standard Control Organisation (CDSCO) can seem daunting. However, with a thorough approach and understanding of the requirements, you can successfully navigate this process. This guide aims to furnish you with the crucial informati

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