Clinical Trials
The Clinical Trials section is responsible for the review, authorization, and oversight of clinical research involving regulated products in Zambia. The Authority ensures that clinical trials are conducted ethically, scientifically, and in accordance with national and international regulatory standards.
This section evaluates trial protocols, investigator qualifications, study documentation, and safety monitoring plans before authorizing the commencement of studies. Throughout the duration of approved trials, ZAMRA monitors compliance to ensure the rights, safety, dignity, and well-being of trial participants are protected.
By facilitating responsible clinical research, the Authority supports scientific innovation and contributes to the development of safe and effective healthcare products for the Zambian population.