Clinical Trials and Regulations are essential pillars of modern medical research, playing a critical role in the development and approval of new drugs, medical devices, therapies, and treatment strategies. These structured processes ensure that emerging medical innovations are thoroughly evaluated for safety, efficacy, and scientific validity before being introduced to the public.
Clinical Trials are systematic research studies conducted with human participants to address specific questions related to medical interventions. They are designed to assess the safety profile, therapeutic effectiveness, optimal dosage, and potential side effects of new treatments or technologies. By following rigorous scientific and ethical standards, clinical trials generate reliable evidence that supports regulatory decisions and advances patient care worldwide.
