Two-day training program on “Designing & Conducting Clinical Trials” by ICMR-NITM concludes


BM Bureau, Sept 15 :  Two-day training program on “Designing & Conducting Clinical Trials” organized by and held at ICMR-NITM Belagavi concluded today.  The training programme, convened by Dr Subarna Roy, Director of ICMR-NITM Belagavi aimed to strengthen clinical research capabilities across the health systems. On the concluding day, experts from ICMR-National Institute of Epidemiology, Chennai Dr Rizwan and D . Vignesh discussed the importance of proper sampling and methods of sampling in the conduct of clinical trials. Dr Aparna Mukherjee from ICMR, New Delhi spoke on how research data safety is monitored and ensured. D Jaya Singh Kshatri from ICMR-Regional Medical Research Centre, Bhubaneswar, and Dr Tejas Patel from AIIMS Gorakhpur were among the other speakers.

At the concluding session of the training program, Dr Roy, ICMR-NITM Belagavi connected various aspects of working with integrative medicine with clinical research and conduct of trials. He highlighted the issues pertaining to regulations and provisions for reporting adverse reactions. Dr MS Ganachari spoke on quality control and quality assurance in clinical trials.

The program achieved its goal through very useful interactions and deliberations among the sixty participants and resource persons who came from various disciplines viz., Medicine, Dentistry, Pharmacy, Ayurveda, Homeopathy, Unani, and Basic Sciences. Participants from 11 States participated in the program.

Earlier on Thursday, the program was inaugurated in the presence of Dr Padmapriyadarsini, Director, ICMR-National Institute for Research in Tuberculosis, Chennai, and Dr Shivaprasad Gouder, Director of Research of KLE Academy of Higher Education and Research, Belagavi.

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Photo : The team of scientists and medical research experts after conclusion of the training program.

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