CDSCO Manufacturing License for Medical Devices in India

An in-depth overview of the Central Drugs Standard Control Organization (**[CDSCO][1]**) licensing process for manufacturing medical devices in India. Learn about the application forms (MD-3, MD-7), risk-based device classification (Class A to D), key requirements like the Plant Master File (PMF) and Device Master File (DMF), and compliance with the Medical Devices Rules, 2017

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[1]: https://www.agileregulatory.com/service/medical-device-manufacturer-registration