9. Subject Considerations

6. Biological Specimen

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

7. Decentralized Clinical Trials

5. Investigator and Investigational Product

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

2. General Questions

1. Executive Summary

Regulatory Overview on Food Contact Materials

9. Advertising Aspects

8. Safety Parameters

5. Claim Requirements

3. Compositional Aspects

Recyclability Logos on Product Labels for Food and Beverages

7. Importation Requirements

7. Importation Requirements

6. Registration Processes