MD 42 Certificate – Essential Certification for Medical Devices in India The MD 42 Certificate is a mandatory approval issued by the Central Drugs Standard Control Organization (CDSCO) for the manufacturing and import of specific low-risk Class A and Class B medical devices in India. This certification ensures that the product complies with the Medical Device Rules, 2017, under the Drugs and Cosmetics Act. It covers devices ranging from surgical instruments to diagnostic equipment. At Agile Regulatory, we assist businesses in obtaining MD 42 Certificates smoothly by managing documentation, application filing, and regulatory coordination. Ensure legal compliance and market access in India’s growing healthcare sector with our expert support in medical device certification. Read More : https://www.agileregulatory.com/blogs/what-is-medical-device-wholesale-license-a-comprehensive-guide

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