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Risk-Based Monitoring in Clinical Trials - AD-TEAM - 01-03-2025 Risk-Based Monitoring in Clinical Trials Published 12/2024 MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz, 2 Ch Language: English | Duration: 1h 39m | Size: 890 MB Risk-Based Monitoring, Centralized Monitoring, Clinical Trials, Clinical Research, RBQM What you'll learn Introduction and Background to RBM Principles and Components of RBM Implementations and Considerations in RBM Benefits and Advantages of RBM Guidance from USFDA, EMA and Use of AI/ML in the RBM process Case Studies & Future Direction and Implications Requirements Laptop/ PC/ Cellphone Good Internet connection Basic English Description Course Title: Risk-Based Monitoring in Clinical TrialsCourse Description:Elevate your clinical trial management skills with our specialized course on "Risk-Based Monitoring in Clinical Trials". This course is designed for clinical research professionals, data managers, and anyone involved in clinical trials who wants to implement RBM strategies to enhance trial efficiency and data quality.What You'll Learn:Introduction and Background to RBMPrinciples and Components of RBMImplementations and Considerations in RBMBenefits and Advantages of RBMGuidance from USFDA, EMA and Use of AI/ML in the RBM processCase Studies & Future Direction and Implications.Why Enroll:Expert Instruction: Learn from seasoned professionals with extensive experience in clinical trial monitoring.Flexible Learning: Access course content anytime, anywhere, and learn at your own pace.Certification: Receive a certificate of completion to boost your professional credentials.Interactive Community: Engage with a community of learners and experts to share knowledge and experiences.Who Should Enroll:Clinical research professionalsData managersClinical trial coordinatorsRegulatory affairs specialistsStudents and graduates in life sciencesEnroll now to master "Risk-Based Monitoring in Clinical Trials" and ensure the success and integrity of your clinical trials. See you in the Class.Thanks and Best Regards,PV Drug Safety Academy Who this course is for Clinical research professionals Clinical Data managers Clinical trial coordinators Regulatory affairs specialists Students and Graduates in Life sciences, Pharmacy and Medical background |