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The video titled "FDA Clinical Investigator Training Course (CITC) 2024 – Day Two – Session Two" continues to build on the knowledge gained in previous sessions, focusing on the practical aspects of conducting clinical trials under FDA regulations. This session emphasizes the importance of effective communication among clinical trial teams, the management of trial logistics, and the implementation of quality assurance practices. Participants learn about the critical role of documentation, monitoring, and compliance in ensuring the integrity of clinical data. The training aims to equip clinical investigators with the tools and strategies necessary to navigate the complexities of clinical research while adhering to regulatory standards and ethical guidelines. #FDA, #ClinicalTrials, #ClinicalResearch, #ClinicalInvestigatorTraining, #RegulatoryCompliance, #QualityAssurance, #CITC2024, #TrialLogistics, #ResearchEthics, #ClinicalInvestigator, #GoodClinicalPractice, #DataIntegrity, #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 comprehensive 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. Original link: • FDA Clinical Investigator Training Course ...