Medical Devices Rules 2017

Law Healthcare & Pharma English Drugs and Cosmetics

Date: 4th Oct, 2024 Source: Central Drugs Standard Control Organization Country: India Original Source

Brief

The Medical Devices Rules, 2017 regulate the manufacturing, import, and sale of medical devices in India, focusing on safety and quality. Key provisions include a risk-based classification system, licensing requirements, and clinical investigation protocols. Amendments reflect updates to international standards and technological advances.

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Central Drugs Standard Control Organization

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