Mandatory Registration of the Research Ethics Committees in India
Shubhasis Dan, Balaram Ghosh, Bapi Gorain and T.K. Pal
Affiliation: Bioequivalence Study Centre, Department of Pharmaceutical Technology, Jadavpur University, Kolkata - 700 032, India.
Keywords: CDSCO, ethics committee, licensing authorities, registration, schedule-Y, serious adverse events.
Experiment on human for the purpose of finding new treatment of the emerging ailments is a continuous process.
The regulatory bodies regulate all activities related to human experimentation. Due to increase in research activities
now-a-days, it is not always possible to maintain the equal focus for all the activities through the central regulatory
agency. In order to maintain the stringency, regional Institutional Ethics Committee (IEC) upholds the task of regulating
human experiments in India. To maximize regulatory oversight over the regional IEC and clinical trials in India, Central
Drugs Standard Control Organization (CDSCO) has recently made an amendment to its regulatory guideline (Schedule Y
of the Drug and Cosmetic Act). This amendment mandates the registration of Ethics Committees which will help in the
accountability of the clinical trials approved or reviewed by the IEC. Such an important step in the Indian regulatory will
make a great impact on the Indian clinical research scenario.
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