Entering the Indian market for medical devices presents a unique scenario for manufacturers. To successfully operate in this growing sector, it's crucial to comply with the regulatory framework set by the Central Drugs Standard Control Organization (CDSCO). The CDSCO registration process can seem intricate, but by following a structured approach an… Read More

In India, the Central Drugs Standard Control Organization (CDSCO) regulates medical devices in accordance with the Medical Device Rules 2017 India. For medical CDSCO medical device registration services device registration India on the Sugam portal, one essential requirement is the submission of a Plant Master File (PMF). This document provides det… Read More