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  2. Central Drugs Standard Control Organisation - Wikipedia

    en.wikipedia.org/wiki/Central_Drugs_Standard...

    The Central Drugs Standard Control Organisation (CDSCO) is India's national regulatory body for cosmetics, pharmaceuticals and medical devices.It serves a similar function to the Food and Drug Administration (FDA) of the United States or the European Medicines Agency of the European Union.

  3. Drugs Controller General of India - Wikipedia

    en.wikipedia.org/wiki/Drugs_Controller_General...

    Analysis of Cosmetics received as survey samples from CDSCO (central drug standard control organisation) With the notification of Medical Device Rules 2017 by the Government of India, DCGI will also act as Central Licensing Authority (CLA) for the medical devices which fall under the purview of these rules.

  4. Regulation of therapeutic goods - Wikipedia

    en.wikipedia.org/wiki/Regulation_of_therapeutic...

    Medicines in India are regulated by Central Drugs Standard Control Organization (CDSCO) Under Ministry of Health and Family Welfare. Headed by Directorate General of Health Services(India).CDSCO regulates pharmaceutical products through Drugs Controller General of India (DCGI) at chair. [citation needed] Drugs are classified under five headings.

  5. Is my medical device approved by Medicare? - AOL

    www.aol.com/lifestyle/medical-device-approved...

    List of durable medical equipment covered by Medicare Medically-necessary DME, including blood sugar monitors, hospital beds, and neck braces, are covered by Medicare. Medicare covers DME that ...

  6. List of regulators in India - Wikipedia

    en.wikipedia.org/wiki/List_of_regulators_in_India

    CDSCO – Central Drugs Standard Control Organisation. 1.27 27. IBBI - Insolvency and Bankruptcy Board of India ... Medical Devices and drugs: Central Drug ...

  7. Drugs and Cosmetics Rules, 1945 - Wikipedia

    en.wikipedia.org/wiki/Drugs_and_Cosmetics_Rules...

    "Drugs and Cosmetics Rules, 1945" (PDF). Central Drugs Standard Control Organization.Archived from the original (PDF) on 31 October 2005.; A Review on the Current Classification and Regulatory Provisions for Medicines in Drug & Cosmetic Act, in the light of Present Day Context Recommendations for Drugs & Cosmetics Rules with context of Drug Schedules

  8. List of stringent regulatory authorities - Wikipedia

    en.wikipedia.org/wiki/List_of_stringent...

    A stringent regulatory authority is a regulatory authority which is: a) a member of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), being the European Commission, the US Food and Drug Administration and the Ministry of Health, Labour and Welfare of Japan also represented by the Pharmaceuticals and Medical Devices Agency (as before ...

  9. Medical device - Wikipedia

    en.wikipedia.org/wiki/Medical_device

    The CDSCO classifications of medical devices govern alongside the regulatory approval and registration by the CDSCO is under the DCGI. Every single medical device in India pursues a regulatory framework that depends on the drug guidelines under the Drug and Cosmetics Act (1940) and the Drugs and Cosmetics runs under 1945.

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