Clinical Trials systematically determines the safety and effectiveness of drugs/medications, devices, and diagnostic methods for use in human subjects under proper ethical guidelines issued by the competent authority.

The Institutional Human Ethics Committee of MMCHRI is constituted to scrutinize the clinical study proposals and the same is duly registered with Central Drugs Standard Control Organization (CDSCO) with CDSCO Registration No: ECR/1184/Inst/TN/2019/RR-22.

MMCHRI established an exclusive unit for conducting clinical trials (Clinical Trial Centre) with the purpose of development of a Centre of Excellence for conducting academic and regulatory clinical trials to contribute towards the advancement of medicine and scientific knowledge that would benefit patients and society.

The centre is equipped with a team of highly-qualified research coordinators, who are engaged in the execution of feasibility, protocol preparation, submission of documents to institutional ethics committee, taking informed consent, data collection, statistical analysis and writing scientific manuscripts for publication in peer reviewed journals.