The collection includes comprehensive documents on various aspects of clinical research, emphasizing the critical areas of drug development, regulatory compliance, pharmacovigilance, and methodologies in clinical trials. Topics cover data management practices, safety monitoring, clinical trial design, patient engagement, and recent advancements such as the use of AI. In addition, the documents highlight ethical considerations, guidelines, and the roles of regulatory bodies in ensuring the integrity and safety of clinical studies.
Site Augmentation in Clinical Trials: Accelerating Enrollment Without Adding More Sites
