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- 4. Regulatory Authority (RA)/ Competent Authority (CA)16 Sep 2024
- 5. Investigator and Investigational Product11 Sep 2024
- 3. Ethics Committee (EC) / Institutional Review Board (IRB)11 Sep 2024
- 10. Roadmap of the Submission Process of a Clinical Trial11 Sep 2024
- 9. Subject Considerations11 Sep 2024
- 8. Data Management11 Sep 2024
- 7. Decentralized Clinical Trials11 Sep 2024
- 6. Biological Specimen11 Sep 2024
- 4. Regulatory Authority (RA)/Competent Authority (CA)11 Sep 2024
- 2. General Questions11 Sep 2024
- 1. Executive Summary11 Sep 2024
- 3. Ethics Committee (EC)/ Institutional Review Board (IRB)10 Sep 2024
- 10. Roadmap of the Submission Process of a Clinical Trial10 Sep 2024
- 9. Subject Considerations10 Sep 2024
- 8. Data Management10 Sep 2024
- 7. Decentralized Clinical Trials10 Sep 2024
- 6. Biological Specimen10 Sep 2024
- 5. Investigator and Investigational Product10 Sep 2024
- 2. General Questions10 Sep 2024
- 1. Executive Summary10 Sep 2024