10. Roadmap of the submission process of a Clinical Trial

8. Data management

6. Biological Specimens

5. Investigator and Investigational Product

4. Regulatory Authority (RA)/ Competent Authority (CA)

3. Ethics Committee (EC)/ Institutional Review Board (IRB)

13. Forms & Appendices

12. Resources

9. Subject considerations

7. Decentralized Clinical Trials

2. General Questions

1. Executive Summary

11. Regulatory Overview - DCT Components

Regulatory Status for Use in Dietary Supplements

Regulatory Status for Food Supplements