7. Decentralized Clinical Trials

9. Subject considerations

6. Biological specimen

5. Investigator and Investigational Product

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

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

11. Regulatory Overview - DCT Components

10. Roadmap of the submission process of a Clinical Trial

8. Data management

2. General Questions

1. Executive Summary