8. Data management

9. Subject considerations

5. Investigator and Investigational Product

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

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

10. Roadmap of the submission process of a Clinical Trial

7. Decentralized Clinical Trials

6. Biological specimen

2. General Questions

1. Executive Summary

11. Regulatory Overview - DCT Components

9. Advertising Aspects

8. Safety Parameters

7. Importation Requirements

6. Registration Processes

5. Claim Requirements

4. Labeling Requirements

3. Compositional Aspects

9. Advertising Aspects

8. Safety Parameters