Clinical trials are vital for creating new and improved medications and therapies. Clinical trial data enable doctors and scientists to explore new approaches to disease treatment, management, and prevention.
Following these best practices allows researchers to run clinical trials with integrity, create reliable data, and prioritise participant safety, thereby contributing to the progress of medical knowledge and the discovery of safe and effective therapies.This article examines how clinical research phases protect study volunteers while also ensuring the effective development of new medications and therapies.