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CDSA works on a national mandate to build capacity and capability in clinical development and translational research in India. We, at CDSA, continually strive to bring in interactive learning opportunities for clinical researchers (investigators), ethics committee members, scientists, biomedical researchers, and all other personnel involved in clinical research/trials. The training programs are conducted as per the recommendations of the Training Advisory Committee (TAC).
CDSA is working with key stakeholders like the Indian drug regulators, Central Drugs Standard Control Organisation (CDSCO), Department of Biotechnology (DBT), Biotechnology Industry Research Assistance Council (BIRAC) – National Biopharma Mission (NBM), Department of Science & Technology (DST), National Institute of Biologicals (NIB), Indian Council of Medical Research (ICMR) in augmenting human capital in the area of clinical development.
There are various training areas but the key focus is on current regulatory and ethical requirements for conducting clinical trials in India, Good Clinical Practice, Good Clinical Laboratory Practice, ethical considerations in clinical research, research methodology, novel vaccine development, and immunization policy in a pandemic, regulatory pathways for medical devices, in-vitro diagnostics, phytopharmaceuticals, biopharmaceuticals, vaccines, etc.
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