U.S. Food and Drug Administration (FDA) Guidelines for Conduct of Clinical Trials
The US Food and Drug Administrations (FDA) Good Clinical Practice Program coordinates FDA policies, provides leadership and direction, contributes to international Good Clinical Practice harmonization
activities, plans and conducts training and outreach programs, and serves as a liaison with the HHS Office of Human Research
Protection (OHRP) and other federal agencies and external stakeholders committed to the protection of human research participants.
Listed below are some websites that provide guidance on the conduct of clinical research: