The Central Drugs Standard Control Organization (CDSCO) has released new guidelines for manufacturers. The ones who fall under the category of A&B medical devices (low-risk devices). These Manufacturers must be registered under the new scheme by September 2022. Those who fall under category C & D medical devices were directed to do the same by September 2023.
Intending to implement strict measures relating to the testing and licensing of medical devices, the government is planning to set forth SoPs and guidelines to test medical devices.