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- Post-Market Surveillance: Continuously monitor the device's performance and report any adverse events or issues to CDSCO as required.
- Medical Devices Rules, 2017: These rules under the Drugs and Cosmetics Act, 1940, set out the regulatory framework for the registration and regulation of medical devices in India.
- 2024-08-30Device Description: Detailed description of the medical device, including its intended use, design, and technology.
- Completeness of Application: Well-prepared and complete applications are processed faster. Missing or incomplete documents can cause delays.
- Adherence to Regulations: Ensure compliance with the Drugs and Cosmetics Act, 1940, and Medical Devices Rules, 2017.
- Adherence to Indian Regulations: Ensure compliance with the Drugs and Cosmetics Act, 1940, and the Medical Devices Rules, 2017.
- 2024-08-30Device Description: Detailed information about the device, including its intended use, design, and technology.
- Device Description: Detailed description including intended use, design, and technology.
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