The healthcare sector in India is highly regulated, particularly when it comes to medical devices. One of the most essential regulatory requirements for companies engaged in the wholesale of medical devices is obtaining the MD 42 License Registration Certificate. This license, issued by the Central Drugs Standard Control Organization (CDSCO) under the Ministry of Health and Family Welfare, grants legal authorization for the sale, stock, exhibit, and distribution of medical devices categorized under Class A and B. With the increasing demand for medical devices across hospitals, clinics, and laboratories, this certification has become crucial for wholesalers seeking legitimacy and compliance in the market.

The MD 42 license not only ensures that the business adheres to necessary safety and quality standards but also boosts credibility among clients and partners. To apply for this certificate, businesses must fulfill a range of requirements including appointment of a competent technical person (pharmacist or graduate with appropriate experience), submission of premises details, product listing, and an undertaking to follow Good Distribution Practices (GDP). Applications are submitted online through the CDSCO portal, after which regulatory authorities conduct inspections to ensure that all guidelines are met. Once approved, the license is valid for a specified period and must be renewed before expiration.