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
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