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  2. Pharmacovigilance Programme of India - Wikipedia

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

    The Pharmacovigilance Program makes these reports itself, but ideally, such reports could originate from any clinic. [3] The Pharmacovigilance Programme seeks to encourage a culture and social expectation of reporting drug problems. [3] One of the successes of the program was detecting adverse effects of people in India using carbamazepine.

  3. Society of Pharmacovigilance, India - Wikipedia

    en.wikipedia.org/wiki/Society_of...

    The Society of Pharmacovigilance, India (SoPI), is an Indian national non-profit scientific organisation, which aims at organizing training programmes and providing expertise in pharmacovigilance and enhance all aspects of the safe and proper use of medicines [1]

  4. Pharmacovigilance - Wikipedia

    en.wikipedia.org/wiki/Pharmacovigilance

    Some further PV regulatory examples from the pharmerging nations are as follows. In India, the PV regulatory authority is the Indian Pharmacopoeia Commission, with a National Coordination Centre under the Pharmacovigilance Program of India, in the Ministry of Health and Family Welfare.

  5. Central Drugs Standard Control Organisation - Wikipedia

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

    The Indian government has announced its plan to bring all medical devices, including implants and contraceptives under a review of the Central Drugs and Standard Control Organisation (CDSCO). Within the CDSCO, the Drug Controller General of India (DCGI) regulates pharmaceutical and medical devices and is positioning within the Ministry of ...

  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. Postmarketing surveillance - Wikipedia

    en.wikipedia.org/wiki/Postmarketing_surveillance

    Postmarketing surveillance (PMS), also known as post market surveillance, is the practice of monitoring the safety of a pharmaceutical drug or medical device after it has been released on the market and is an important part of the science of pharmacovigilance.

  8. My best friend and I gave our daughters the same name. We ...

    www.aol.com/best-friend-gave-daughters-same...

    We live in different countries, so we thought the shared name would be a great connection for them. They both decided to change their names, but the bond still exists. I met my best friend in 2005 ...

  9. Category:Regulatory agencies of India - Wikipedia

    en.wikipedia.org/wiki/Category:Regulatory...

    Download as PDF; Printable version; ... Insolvency and Bankruptcy Board of India; ... Pharmacovigilance Programme of India;