On-Demand Training Courses for Clinical Research Professionals
Barnett International offers a wide range of On-Demand Training Courses designed to meet your training needs within your busy schedule. Take a course at your own pace while completing immersive core competency learning modules, pre-testing, and post testing. On-Demand courses are also ideal for bringing your entire team up to speed on a particular topic area, allowing more familiar team members to test-out and continue with their day-to-day requirements.
Course Customization
All of Barnett's On-Demand eLearning courses can be customized to meet your specific needs, such as SOP integration, logo inclusion, etc.
Course Licensing
All of Barnett's On-Demand eLearning courses can be licensed and integrated into your Learning Management System.
For more details contact Barnett today!
Good Clinical Practice for Sponsors & Service Providers
Barnett’s new ICH GCP E6(R3) course covers the essential elements of ICH GCP requirements. It is designed for sponsor and service provider personnel seeking a detailed review of the guideline's content and application. This comprehensive and interactive course can be taken at your own time and pace. For experienced individuals, each section provides a “test-out” option to focus on new content and areas where refresher training may be needed.
Key Features of the Course Include:
- Interactive modules aligned with the core areas and requirements outlined in ICH E6(R3)
- Situational-based learning content and scenarios that align with challenges that clinical researchers encounter regularly in their roles
- Emphasis on what is new in the R3 release (Jan 2025) of ICH E6
- Knowledge assessments and case study reviews throughout the course
- Downloadable References, Glossary and Acronyms guides
- 2025 Good Clinical Practice training certificate
Course Learning Objectives:
Upon completion of the course, you will be able to:
- Describe the foundations, background and application of E6(R3)
- Identify the key changes in E6(R3)
- Describe the roles and responsibilities of the IRB/IEC, investigator, sponsor and service providers with respect to the planning, conduct and oversight of clinical trials
- Identify some of the regional regulations that govern clinical trials
- Appreciate the importance of compliance to E6(R3) and explain the impact of noncompliance
- Apply your knowledge of E6(R3) by completing tests and challenges (based on course content)
Additional Benefits of the Course:
- Know the key regulations governing the conduct of clinical trials, including common Audit and Inspection findings
- Understand ICH GCP E6(R3) Principles, Content and Structure (including what is new)
- Describe the expectations for the Institutional Review Board (or IRB) or Independent Ethics Committee (or IEC)
- Review the detailed expectations of the Investigator, the Sponsor and Service Providers
- Know requirements for Informed Consent, Investigational Product Management, the Protocol (including Deviations management) and the Investigator Brochure throughout the lifecycle of trials
- Define Sponsor Quality Management requirements including Risk Management, Quality Assurance, Quality Control and Monitoring
- Know the standards required to ensure that the trial-related Data and Records are fit for purpose
- Describe requirements and proper management and Reporting of Safety Events (including common deficiencies)
- Understand Data Governance requirements and the appropriate management of Data Integrity, Traceability and Security to ensure accurate reporting
- Explain requirements for the management of Computerized Systems used in clinical trials by responsible parties
- Describe requirements for the management of Essential Records that are generated throughout a clinical trial
- Practice what you’ve learned through knowledge checks and application-based case studies
Sample Challenge Scenarios Included in the Course:
- Identify the trial oversight tasks are appropriate to delegate when outsourcing to a CRO/Service Provider
- Choose the actions that should be taken when dosage-related noncompliance is detected
- Consider protocol amendment variables requiring updates to the informed consent form
- Decide which sites should be selected by reviewing site qualification findings
- Identify the steps that should be taken when significant noncompliance is detected
- Assign the activities that apply to each role specific to IRB/IEC procedures
- Decide what could be included as a critical to quality factor
- And many more…!
Course Module Structure:
Flexible Training Options:
The course is available for Individuals and Team/Organizational Training :
Barnett can host and manage enrollment for individuals and teams. The more participants you register, the lower the cost per user.
1-10 Users $199 per user
11-20 Users $179 per user
21-30 Users $169 per user
31-40 Users $159 per user
41+ Users $149 per user
License the course and seamlessly integrate it into your organization’s Learning Management System (LMS)
For Group Training and Licensing Partners, Course Demos are Available
For an additional fee, the course can be customized to meet your organization’s specific needs, such as company specific examples, logo/branding inclusion, and more.
For more information, contact Barnett at:
Customer.service@barnettinternational.com
To inquire about licensing this course for inclusion in your LMS, contact:
nganatra@barnettinternational.com
WHAT OUR CUSTOMERS SAY
Thank you! I have completed the training and generated my certificate. I think Barnett’s Good Clinical Practice for Sponsors and CROs was the most thorough GCP training I’ve ever taken!"
- Barnett On-Demand GCP For Sponsors and CROs course graduate
