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The CTRI requests all the information which the World Health Organization recommends for clinical trial registries. [8] Additionally, the CTRI collects information specific to the circumstances of India, including the address of the principal investigator, the name of the ethics committee overseeing the trial and confirmation of their government registration; proof of permission from the Drugs ...
The DRKS is an open access, free of charge online register for clinical trials and is available both in English and German. DRKS is part of the WHO's ICTRP. The DRKS works with two partner registries in Germany, DeReG (German Registry for Somatic Gene-Transfer Trials) and Clinical Trial Registry of the University Medical Center Freiburg. [4]
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.
The ICMR is funded by the Government of India through the Department of Health Research, Ministry of Health and Family Welfare. [2] [3] In 2007, the organization established the Clinical Trials Registry - India, which is India's national registry for clinical trials. [4]
The International Clinical Trials Registry Platform (ICTRP) is a platform for the registration of clinical trials operated by the World Health Organization. [1]The ICTRP combines data from multiple cooperating clinical trials registries to generate a global view of clinical trials worldwide, with a search portal that allows access to the entire dataset.
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The Clinical Establishments (Registration and Regulation) Act, 2010 is an Act of the Parliament of India.It seeks to regulate all clinical establishments in India. On April 15, 2010, the Clinical Establishments (Registration and Regulation) Bill, 2010 was introduced in the Lok Sabha for the first time.
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