MD 42 Registration for Medical Devices – Process & Compliance Guide

MD 42 registration is mandatory for manufacturers and importers of non-invasive medical devices under India's Medical Device Rules, 2017. This license ensures compliance with safety, efficacy, and regulatory standards set by CDSCO. At Agile Regulatory, we assist in documentation, online portal submission, and end-to-end guidance for a hassle-free MD 42 registration process.

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