The FDA provides oversight for clinical trials of investigational drugs, biologic products and medical devices.
- Running clinical trials
- FDA educational materials
- FDA compliance and enforcement information
- FDA alerts
Clinical trials involving investigational drugs, biologics and/or devices are governed by specific FDA regulations. Numerous parties involved in the clinical trials process, including study sponsors, principal investigators and institutional review boards, are subject to applicable FDA regulations.
- FDA regulations related to good clinical practice and clinical trials
- Electronic records; electronic signatures 21 CFR 11
- Protection of human subjects 21 CFR 50
- Financial disclosure by clinical investigators 21 CFR 54
- Institutional review boards 21 CFR 56
- Investigational new drug application 21 CFR 312
- Investigational device exemptions 21 CFR 812
FDA guidance documents and information sheets
The FDA provides guidance documents that describe the FDA's current thinking about issues related to FDA-regulated clinical trials. In addition, the FDA publishes information sheets that provide guidance and recommendations for IRBs, clinical investigators and sponsors to help them fulfill their responsibilities to protect human subjects who participate in FDA-regulated research.
- Guidance for industry: Investigator responsibilities-protecting the rights, safety and welfare of study subjects
- FDA guidance for clinical investigators, sponsors and IRBs: Adverse event reporting to IRBs - improving human subject protection
- Financial disclosure by clinical investigators
- ICH GCP E6 - Good clinical practice: Consolidated guidance
Guidance on clinical trial registration on ClinicalTrials.gov
- Certification requirements to accompany drug, biologics and device submissions in association with Clinical Trial Registrations
FDA compliance findings
The most recent FDA warning letters can be accessed on the FDA website.
Lauren Wallace, MS, RAC-Drugs
Director of clinical research regulatory affairs