10. Roadmap of the Submission Process of a Clinical Trial

9. Subject Considerations

11. Regulatory Overview - DCT Components

7. Decentralized Clinical Trials

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

5. Investigator and Investigational Product

8. Data Management

6. Biological Specimen

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

2. General Questions

1. Executive Summary

Overview of Sustainability Requirements for Packaging

Overview of Packaging Legislation in Germany

8. Safety Parameters

7. Importation Requirements

6. Registration Processes

5. Claim Requirements

4. Labeling Requirements

3. Compositional Aspects

2. Product Categories