AI in Action: Shaping the Future of Oncology Clinical Research

November 18, 2026—This live webinar explores practical applications of AI in oncology trials, focusing on three high-impact areas: 1) patient matching and identification using advanced algorithms to accelerate enrollment and improve diversity; 2) seamless data collection through integration from electronic medical records to electronic data capture, reducing manual errors and increasing efficiency; and 3) automated imaging analysis, such as AI-driven RECIST measurements, to improve consistency and speed in response assessments.

ICH E6(R3) Explained: From Regulatory Principles to Clinical Trial Practice

December 2, 2026—This sponsored webinar by Agatha Life Sciences will provide an accessible overview of ICH E6(R3), explaining the rationale behind the revision, its core principles, and the key changes clinical research professionals should understand. Particular attention will be given to areas such as Quality by Design, risk-proportionate approaches, data governance, computerized systems, roles and responsibilities, and essential records.

Participant Compensation in Clinical Research: How Much Is Too Much?

January 27, 2027—This live webinar will examine the ethical and regulatory considerations surrounding participant reimbursement, compensation, and incentives in clinical research. Participants will explore how payment amounts, structures, and delivery methods can influence enrollment, retention, participant reporting, and access to research opportunities.

2026 ACRP and Academy Annual Membership Meeting

ACRP Leadership shared how we’ve worked to advance the clinical research profession over the past year. We shared a full picture of where we’ve been, highlighted our 50th Anniversary year, and shared what’s ahead for 2027.

​​Risk‑Based Decisions: Key Skills for Ensuring Quality Control Under ICH E6(R3) Guidance​

Aligned with the latest ICH GCP E6(R3) principles, this course provides practical strategies for applying risk-based quality management (RBQM) approaches and focusing resources where they can have the greatest impact. Learn how to identify, assess, prioritize, and manage risks using Critical-to-Quality (CtQ) factors, while incorporating Quality by Design (QbD) principles into trial planning and conduct.