The National Institute for Medical Research (NIMR), in collaboration with the Tanzania Medicines and Medical Devices Authority (TMDA), on 24th November 2025 conducted a specialized capacity-building training for Clinical Trials researchers under the “Trial Regulation and Clinical Ethics Optimization (TRACE) in Africa” Project.

Speaking during the opening of the three-day training, NIMR Director General, Prof. Said Aboud, said that clinical trials continue to become more complex as technology rapidly evolves, requiring highly skilled professionals as well as strong ethical and regulatory frameworks to guide their implementation.

Prof. Aboud emphasized that NIMR is committed to strengthening the national clinical research system to ensure it aligns with current scientific demands and international standards.

“These trainings go beyond classroom learning. They incorporate interactive approaches, including practical simulations and case analysis, to enhance decision-making skills, identify ethical gaps, and ensure compliance with regulatory requirements,” he added.

The TRACE Project aims to deliver four major outcomes: strengthening ethics and regulatory capacity, improving efficiency and speed in reviewing clinical trial applications, enhancing quality in trial oversight and monitoring, and promoting collaboration, information access, and positive research impact across the country.

Prof. Aboud urged participants to make full use of the training and return to their institutions as ambassadors of high professional and ethical standards in the conduct of clinical trials.