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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. Drugs Controller General of India - Wikipedia

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

    Drugs Controller General of India (DCGI) is the head of department of the Central Drugs Standard Control Organization of the Government of India responsible for approval of licences of specified categories of drugs such as blood and blood products, IV fluids, vaccines, and sera in India. Drugs Controller General of India, comes under the ...

  4. Pharmacovigilance Programme of India - Wikipedia

    en.wikipedia.org/wiki/Pharmacovigilance...

    cdsco.gov.in /opencms /opencms /en /PvPI /. The Pharmacovigilance Programme of India (PvPI) is an Indian government organization which identifies and responds to drug safety problems. [1] Its activities include receiving reports of adverse drug events and taking necessary action to remedy problems. [1] The Central Drugs Standard Control ...

  5. Clinical Trials Registry – India - Wikipedia

    en.wikipedia.org/wiki/Clinical_Trials_Registry...

    Clinical Trials Registry – India (CTRI) is the government of India's official clinical trial registry. The National Institute of Medical Statistics of the Indian Council of Medical Research established the CTRI on 20 July 2007. [1] Since 2009 the Central Drugs Standard Control Organisation has mandated that anyone conducting clinical trials ...

  6. Clinical trials in India - Wikipedia

    en.wikipedia.org/wiki/Clinical_trials_in_India

    Clinical trials in India refers to clinical research in India in which researchers test drugs and other treatments on research participants.NDCTR 2019 and section 3.7.1 to 3.7.3 of ICMR guidelines [1] requires that all researchers conducting a clinical trial must publicly document it in the Clinical Trials Registry - India.

  7. Drugs and Cosmetics Act, 1940 - Wikipedia

    en.wikipedia.org/wiki/Drugs_and_Cosmetics_Act,_1940

    The Drugs and Cosmetics Act, 1940 is an act of the Parliament of India which regulates the import, manufacture and distribution of drugs in India. [1] The primary objective of the act is to ensure that the drugs and cosmetics sold in India are safe, effective and conform to state quality standards. [2] The related Drugs and Cosmetics Rules ...

  8. Drugs and Cosmetics Rules, 1945 - Wikipedia

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

    An act to regulate import, manufacture, distribution and sale of Drugs and Cosmetics. The Drugs and Cosmetics Rules, 1945 are the rules which the government of India established for the implementation of the Drugs and Cosmetics Act, 1940. These rules classify drugs under given schedules and present guidelines for the storage, sale, display and ...

  9. ZyCoV-D - Wikipedia

    en.wikipedia.org/wiki/ZyCoV-D

    COVID-19 portal. v. t. e. ZyCoV-D is a DNA plasmid -based COVID-19 vaccine developed by Indian pharmaceutical company Cadila Healthcare, with support from the Biotechnology Industry Research Assistance Council. It is approved for emergency use in India.