Clinical Trials Regulation

Clinical Trials Regulation refers to the set of rules that govern how medical research is conducted to ensure the safety and rights of participants while also promoting scientific integrity. These regulations require that trials are conducted ethically, with informed consent from participants, and that their results are reported transparently. This framework helps ensure that new treatments and interventions are tested rigorously before being approved for public use, balancing the need for innovation in medicine with the protection of individuals involved in the research.