We are pleased to share this important update with our ACRP Certified community.
In response to stakeholder feedback, the Association of Clinical Research Professionals (ACRP) is accelerating its timeline for incorporating the updated ICH Guideline for Good Clinical Practice E6(R3) into all ACRP Certification examinations.
Originally announced in February 2025, the integration was planned over a two-year period following the guideline’s final adoption on January 6, 2025. However, based on strong interest in earlier adoption, ACRP has begun the work to incorporate E6(R3) into its exams ahead of schedule.
Beginning with the spring 2026 testing window (February 15 – May 15), candidates will encounter a set of unscored pre-test questions referenced to the new E6(R3) guideline. These items will not affect candidate scores but will allow ACRP to gather essential statistical data to support instant scoring during the fall 2026 testing window (July 15 – October 15), which will be fully referenced to E6(R3).
This means that starting on July 15, 2026, candidates will be expected to understand and apply the updated E6(R3) guideline as it relates to the Examination Content Outline (ECO) for their ACRP Certification exam.
ACRP remains committed to ensuring its certification programs reflect current industry standards and best practices. We continue to encourage candidates to engage in continuing education related to the ICH GCP E6(R3) update to support their professional development and exam readiness. ACRP members benefit from the lowest rates on continuing education, training courses, and maintenance of certification.
If you have questions about ACRP Certification, ICH E6(R3) training courses, or the benefits of membership, please contact ACRP Customer Care.
ACRP’s Recently Released ICH E6(R3) Training Courses:
- Good Clinical Practice (GCP) ICH E6(R3) – ACRP’s Foundational Training Course
- Clinical Trials 101: An Introduction with ICH E6(R3) Guidance (January 2026)
- eResearch in Practice: Managing Clinical Trials with ICH E6(R3) Guidance
- Ethics and Human Subject Protection: An Introduction with ICH E6(R3) Guidance
- Ethical Foundations in Clinical Trials: A Refresher with ICH E6(R3) Guidance
- Form FDA 1572 Essentials: Updated for ICH E6(R3)
- Informed Consent Scenarios with ICH E6(R3) Guidance
- Understanding Clinical Trial Protocols Under ICH E6(R3) Guidelines (January 2026)



