Clinical Trials Registry India (CTRI)
- July 5, 2021
- Posted by: OptimizeIAS Team
- Category: DPN Topics
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Clinical Trials Registry India (CTRI)
Subject: Governance / Science & tech
Context: Recently, the Ministry of AYUSH has announced that the Ayurveda Dataset on Clinical Trials Registry India (CTRI) Portal will be launched.
Concept:
- The Ayurveda Dataset of CTRI has been jointly developed by ICMR and Central Council for Research in Ayurvedic Sciences (CCRAS), Ministry of Ayush.
- Its key feature is the provision of selection of the Ayurveda Health conditions from drop down of 3866 Ayurveda morbidity codes incorporated from the NAMASTE portal.
- It provides that the information, results etc. of Ayurveda Clinical Trials will be available in Ayurvedic vocabulary in the clinical trials registry of India.
Clinical Trials Registry India (CTRI)
- It is a primary register of Clinical Trials under WHO’s International Clinical Trials Registry Platform (ICTRP).
- It hosted at the ICMR’s National Institute of Medical Statistics (NIMS).
- It is a free and online public record system for registration of clinical trials being conducted in India.
- It was initiated as a voluntary measure since 2009.
- The trial registration in the CTRI has been made mandatory by the Drugs Controller General (India) (DCGI).
International Clinical Trials Registry Platform (ICTRP)
- It is a project of the World Health Organization, based within the Health Metrics and Measurement cluster.
- It was established in August 2005.
- It is based in WHO Headquarters in Geneva, Switzerland.
- Its aim is to facilitate the prospective registration of the WHO Trial Registration Data Set on all clinical trials, and the public accessibility of that information.
- Its purpose is to strengthen accountability and transparency in the conduct of clinical research and dissemination.