Navigating the regulatory landscape of medical device distribution in India is crucial for ensuring compliance and building trust with consumers. The MD 42 License, as mandated by the Ministry of Health and Family Welfare's 5th Amendment of Medical Device Rules, is essential for retailers, wholesalers, and stockists engaged in selling, stocking, exhibiting, or distributing medical devices, including in-vitro diagnostics. Effective from September 30, 2022, obtaining this registration certificate is a legal requirement. Our consultancy specializes in guiding businesses through the MD 42 licensing process, ensuring adherence to Good Distribution Practices and facilitating a smooth application experience. 

Address : D- 215 Sector-63, Noida, UP, 201301

Phone No : 8178731176 Website : https://www.agileregulatory.com/service/factory-license-process