When.com Web Search

  1. Ads

    related to: approved medical devices cdsco

Search results

  1. Results From The WOW.Com Content Network
  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. 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.

  4. 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.

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

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

    If a person has Original Medicare, Part B covers 80% of the approved cost after they meet the deductible of $240. For someone with Medicare Advantage, the out-of-pocket costs vary with the plan.

  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. 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 ...

  1. Ad

    related to: approved medical devices cdsco