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The video titled "FDA Clinical Investigator Training Course (CITC) 2024 – Day Two – Session One" focuses on advanced topics relevant to clinical investigators in the context of FDA regulations. This session delves into the intricacies of clinical trial design, data management, and the importance of maintaining compliance throughout the research process. Participants learn about the roles of various stakeholders in clinical trials, the significance of monitoring and reporting adverse events, and the ethical considerations that must be upheld. This training is crucial for ensuring that clinical investigators are well-prepared to conduct high-quality research that adheres to regulatory standards and prioritizes participant safety. #FDA, #ClinicalTrials, #ClinicalResearch, #ClinicalInvestigatorTraining, #RegulatoryCompliance, #DataManagement, #CITC2024, #AdverseEvents, #ResearchEthics, #ClinicalInvestigator, #GoodClinicalPractice, #DrugDevelopment, #ResearchTraining, #Biologics, #MedicalDevices Rationale for Sharing the Original Link We are sharing the original link to provide viewers with direct access to the complete training session, which offers in-depth insights and expert guidance from FDA professionals. This ensures proper attribution to the original creators and allows our audience to explore the full context of the training material. By linking to the original video, we promote transparency and encourage further learning about FDA regulations and best practices in clinical research. The original session includes detailed discussions and examples that enhance understanding of the topics covered, making it a valuable resource for clinical investigators and researchers. • FDA Clinical Investigator Training Course ...