Thank you for joining Critical Path Clinical Connect eTMF Learning Series! Inspection Readiness is critical to the success and quality of your clinical program. Proactive planning will ensure smoother, instream collection and frequent quality checks to remain inspection ready at all times. This comprehensive training program is designed to equip participants with the essential knowledge and skills needed to effectively manage Electronic Trial Master Files (eTMF). In today's dynamic clinical research landscape, where regulatory compliance and data integrity are paramount, proficiency in eTMF management is indispensable for all stakeholders involved in clinical trials. Throughout this course, participants will delve into the fundamentals of eTMF management, exploring topics such as document organization, regulatory requirements, quality control measures, and best practices for ensuring data accuracy and completeness. Practical insights and real-world case studies will be utilized to illustrate key concepts and reinforce learning. 1. Understand the purpose and importance of eTMF in clinical trials. 2. Familiarize with regulatory guidelines governing eTMF management. 3. Learn effective strategies for organizing and maintaining eTMF documentation. 4. Develop proficiency in using eTMF systems and software. 5. Explore quality control measures to ensure data accuracy and completeness. 6. Gain insights into inspection readiness and audit preparation. 7. Understand the role of eTMF in facilitating collaboration among trial stakeholders. 8. Identify common challenges and best practices for overcoming them in eTMF management. By the end of this training, participants will emerge with the knowledge and skills needed to navigate the complexities of eTMF management confidently, ensuring compliance, efficiency, and data integrity throughout the clinical trial process.