RBQM Essentials – Green Belt, e-Course

A self-paced learning experience designed for individual learners and groups, complete in less than 6 hours!

Our Green Belt e-course is based on real-world clinical study data, making it a unique learning experience for clinical research professionals leading clinical trials or serving as study team members. This comprehensive program allows you to master the fundamentals of advanced aspects of risk-based quality management methodology. With this real-world data approach, you’ll excel in risk detection, evaluation, control, communication, review, and reporting, in line with ICH Good Clinical Practice E6(R2) in less than 6 hours.


Welcome to RBQM Essentials ‘Green Belt’: Your Path to Success

Embark on a journey of discovery with our Green Belt e-course, specifically designed for clinical research professionals who are either leading clinical trials or serving as integral members of study teams. This comprehensive, self-paced program allows you to master both the fundamental and advanced aspects of Risk-Based Quality Management (RBQM) methodology, unveiling the secrets of RBQM that can lead you to success in your professional journey.

Self-Paced E-Course

Our Green Belt e-course is a unique learning experience, grounded in real-world clinical study data provided by Cyntegrity. This self-paced learning module allows you to delve deep into the intricacies of RBQM at your own convenience, ensuring a thorough and comprehensive understanding of the methodology. The course is designed to be completed and certified in less than 6 hours, making it a highly convenient and efficient solution for busy professionals seeking to enhance their knowledge and skills.

“We are happy with the engagement and level of knowledge that MyRBQM Academy brought to our Operations teams as to the RQBM implementation. And, by using Cyntegrity’s unique RBQM technology we were able to retrospectively analyze a real world clinical study and conduct a workshop to successfully generate new ideas for further improvements on a global scale,” said Jens Opitz, Executive Director, Head of Global Clinical Operations at Merz Pharmaceuticals GmbH. Read also: Merz Pharma’s RBQM Journey published by Applied Clinical Trials

Green Belt Certification and Quiz

This RBQM Essentials course culminates with a certification quiz, designed to test your understanding and mastery of RBQM concepts. This exam ensures that you have acquired the necessary knowledge to effectively apply RBQM principles in your clinical research practice, thereby enhancing your professional credibility.

Boost Your Clinical Research Career

The RBQM Essentials Green Belt training offers a unique opportunity to advance your clinical research career. With a deeper understanding of RBQM methodology, you’ll be better equipped to manage risks and ensure compliance in the industry.

Completing the Green Belt training allows you to unlock your risk management potential, make informed decisions, effectively manage risks, and contribute to your organization’s clinical trial success.

Unique Learning Experience

Our e-course combines lessons and case studies, enabling you to apply RBQM in daily practice. Learn at your own pace while engaging in a unique knowledge-sharing experience.

RBQM Essentials Belt Courses

  • ICH E6 & E8 Guidelines: Understanding their implications in clinical research
  • RBQM Objectives: Delving into the goals of Risk-Based Quality Management
  • Critical Processes & Data: Identifying the vital elements in clinical trials
  • Risk Identification: Uncovering potential challenges and pitfalls
  • Risk Evaluation: Assessing the severity and impact of identified risks
  • Risk Control: Implementing strategies for managing and mitigating risks
  • Issue Management: Analyzing root causes and preventing recurrence
  • Risk Communication: Ensuring key stakeholders are informed about risks
  • Risk Review: Examining and updating risks throughout the trial
  • Risk Reporting: Documenting risks in the Clinical Study Report (CSR)
  • RBQM Summary: Consolidating your understanding of RBQM principles
  • Hands-on Exercise: Attain proficiency in the pivotal facets of RBQM! Augment your recently acquired expertise and competencies, effectively using them through hands-on exercises based on clinical study data provided by Cyntegrity

Who should attend?

  • Risk Managers
  • Study Managers
  • Central Monitors
  • Lead Biostatisticians
  • Lead Data Managers
  • Medical Monitors
  • CQA Representatives/Auditors
  • Lead CRAs
  • Site Start Up/Regulatory Leads
  • Safety Leads
  • Medical/Scientific Affairs

NOTE: Prior MyRBQM® Academy White Belt certification is required; however, this prerequisite can be skipped if you successfully pass the prequalification quiz, allowing you to enroll directly in the Green Belt course. Request for the Green Belt prequalification quiz: academy@cyntegrity.com

Why should you attend?

  • Boost Your Skillset: Obtain your Green Belt certification and propel your career forward in clinical research, demonstrating your proficiency in RBQM methodology and Risk-Based Monitoring.
  • Achieve Regulatory Compliance: Master the essential techniques to ensure compliance in your industry, safeguarding your organization’s reputation and credibility.
  • Exclusive Community: Gain access to the distinguished MyRBQM® Academy Alumni community, networking with like-minded professionals and industry leaders who share your passion for excellence.
  • Valuable Bonuses: Maximize your learning experience with exclusive bonuses like the Risk Management Plan Tool and Cyntegrity’s Golden KRI Set, providing you with powerful resources to enhance your knowledge and skills.
  • Comprehensive Training: Engage in a captivating self-paced e-course, covering core to advanced elements of Risk-Based Quality Management methodology. Complete the course in your own time and get certified in less than 6 hours.
  • Unleash Your Potential: As a Green Belt, you’ll be equipped to make significant contributions to your clinical study team, elevating your performance and driving improvements in your organization’s clinical trials.


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