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  2. Central Drugs Standard Control Organisation - Wikipedia

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

    Website. cdsco.gov.in and www.cdscoonline.gov.in. 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. Medical device - Wikipedia

    en.wikipedia.org/wiki/Medical_device

    The design of medical devices constitutes a major segment of the field of biomedical engineering. The global medical device market was estimated to be between $220 and US$250 billion in 2013. [4] The United States controls ≈40% of the global market followed by Europe (25%), Japan (15%), and the rest of the world (20%).

  4. 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

  5. Drugs Controller General of India - Wikipedia

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

    The government earlier on 14 August 2019 appointed Dr. VG Somani as Drug Controller General of India (DCGI). Dr. VG Somani succeeded S Eswara Reddy, the interim DCGI who was appointed in February 2018. DCGI heads the Indian drug regulatory body the Central Drugs Standard Control Organisation (CDSCO), whose functions include ensuring the quality ...

  6. Regulation of therapeutic goods - Wikipedia

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

    The regulation of therapeutic goods, defined as drugs and therapeutic devices, varies by jurisdiction. In some countries, such as the United States, they are regulated at the national level by a single agency. In other jurisdictions they are regulated at the state level, or at both state and national levels by various bodies, as in Australia.

  7. Drugs and Cosmetics Act, 1940 - Wikipedia

    en.wikipedia.org/wiki/Drugs_and_Cosmetics_Act,_1940

    The term "drug" as defined in the act, includes various substances, diagnostic, and medical devices. The act defines "cosmetic" as any product that is meant to be applied to the human body for the purpose of beautifying or cleansing. The definition however excludes soaps. In 1964, the act was amended to include Ayurveda and Unani drugs. [2]