Course Description

Clinical Data Management (CDM) plays a pivotal role in the success of clinical trials, ensuring data accuracy, integrity, and compliance with regulatory requirements. The ICH GCP E6 R3 update refines the approach to CDM by incorporating a risk-based framework for managing data and enhancing oversight mechanisms. This web seminar will explore the updated guidelines, focusing on the evolving requirements for electronic systems, data integrity, and the integration of quality management principles throughout the trial lifecycle. Participants will gain insights into the role of risk management in clinical data collection and analysis, now positioned as a standard practice rather than an optional strategy. The session will also cover best practices, industry standards, and practical approaches to achieving compliance with the revised guidelines. Additionally, the seminar will highlight the implications of the R3 updates and how they reshape CDM processes, ensuring data quality and regulatory adherence.

Learning Objectives

• Define the recommended SOPs for electronic systems used to collect and manage clinical trial data under ICH GCP E6 R3
• Discuss data integrity considerations and their critical role in clinical trials, as outlined in the revised guidelines
• Identify risk management principles in clinical trial conduct and their direct connection to Clinical Data Management practices
• Review quality management principles and tools to implement a risk-based quality approach in clinical trials

Who Should Attend

• Clinical Data Managers
• Clinical Data Scientists
• Clinical Quality Assurance Professionals
• Clinical Compliance Personnel

Instructor

Denise G. Redkar-Brown, MT

Click here for complete trainer biographies

Registration Fees

$735*

*Includes up to 20 participants per login at a single location. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional logins for other locations, please call +1 781.972.5400 or toll-free in the U.S. 800.856.2556, or email customer.service@barnettinternational.com for pricing.

Accreditation Information

Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.  Participants will receive 1.5 hours (0.15 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation.  Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion.  ACPE#: 0778-0000-25-032-L99-P. Released: 4/25. 

Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.