Regulatory Overview on Food Contact Materials

7. Decentralized Clinical Trials

5. Investigator and Investigational Product

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

2. General Questions

10. Roadmap of the Submission Process of a Clinical Trial

9. Subject Considerations

8. Data Management

6. Biological Specimen

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

1. Executive Summary

GOS in Food - New Zealand

5. Claim Requirements

9. Advertising Aspects

8. Safety Parameters

7. Importation Requirements

6. Registration Processes

4. Labeling Requirements

3. Compositional Aspects

2. Product Categories