Understanding CDSCO MD 7 and MD 9: Key to Medical Device Compliance in India

Navigating India’s medical device regulations requires a deep understanding of CDSCO’s classifications, especially MD 7 and MD 9. This guide from Operon Strategist explains how these forms impact device approval based on risk classes (A to D), and outlines the entire licensing process—from facility setup and documentation to inspections and post-licensing obligations. Ideal for manufacturers entering the Indian market or seeking regulatory clarity.
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