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- 8. Safety Parameters26 Mar 2025
- Hygiene Standards for FCM26 Mar 2025
- Packaging Requirements for FCM26 Mar 2025
- 4. Labeling Requirements24 Mar 2025
- 5. Claim Requirements24 Mar 2025
- 3. Compositional Aspects24 Mar 2025
- 9. Advertising Aspects24 Mar 2025
- 7. Importation Requirements24 Mar 2025
- 6. Registration Processes24 Mar 2025
- 2. Product Categories23 Mar 2025
- 1. Authorities23 Mar 2025
- Tax Policy on Alcohol19 Mar 2025
- Duty-free Requirements for Food Supplements10 Oct 2024
- 7. Decentralized Clinical Trials22 May 2024
- 4. Regulatory Authority (RA)/Competent Authority (CA)21 May 2024
- 6. Biological Specimen21 May 2024
- 3. Ethics Committee (EC)/Institutional Review Board (IRB)21 May 2024
- 10. Roadmap of the Submission Process of a Clinical Trial21 May 2024
- 9. Subject Considerations21 May 2024
- 8. Data Management21 May 2024