MD 42 Certificate – CDSCO Registration for Medical Devices in India
The MD 42 Certificate is mandatory for manufacturers and importers of non-notified medical devices in India under CDSCO regulations.

The MD 42 Certificate is mandatory for manufacturers and importers of non-notified medical devices in India under CDSCO regulations. This certification ensures that your products comply with safety and performance standards before entering the Indian market. Agile Regulatory assists in end-to-end documentation, submission, and compliance for obtaining MD 42 certificates smoothly and efficiently.


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Anil Shinde is a dedicated Regulatory Compliance Specialist at Agile Regulatory, helping businesses navigate complex licensing and certification processes in India. With expertise in BIS certification, factory licensing, pollution control board approvals, and business registrations, Anil ensures seamless compliance for manufacturers, importers, and service providers.

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