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India

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Product Registration

MEDICAL DEVICE REGULATION IN INDIA


Medical devices are regulated by the Central Drugs Standard Control Organization (CDSCO) in India whose objective is to safeguard and enhance the public health by assuring the safety, efficacy, and quality of medical devices. Medical devices are regulated under the Drugs and Cosmetics Act 1940.


MEDICAL DEVICE REGISTRATION AND APPROVAL IN INDIA


Medical devices are classified into 2 categories namely: Notified Medical Devices and Non-notified Medical Devices.

The list of Notified Medical Devices is listed in CDSCO requirement and registration is required for these devices.

Example Of Approval

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Medical device regulatory guidelines
Product Registration
License Holding
Extra RA/QA Suppprt
License Holding

ASEAN / Asia REP

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Extra RA/QA Support

MONTHLY REGULATORY SUPPORT FOR REGIONAL REGISTRATION

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Drug Services
Drug Services

THERAPEUTIC AND COSMETIC APPROVAL

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Health Safety
Health Safety

WIRELESS, RADIATION AND PACKAGING APPROVAL

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