The Association of Clinical Research Professionals

A Review of ICH E8 (R1) General Considerations for Clinical Trials

This recorded webinar reviews the international harmonized standard for pharmaceuticals used in human clinical studies.

This standard guides the clinical development lifecycle including quality requirements for clinical study designs and data sources. Principles and practices for the conduct of clinical trials will be reviewed.

Upon completion of this continuing education program, attendees should be able to:

  • Understand general considerations for clinical trials
  • Describe clinical trial development plans
  • List phases of clinical development

Joy Frestedt, PhD, CPI, RAC, FRAPS, FACRP, President/CEO, Frestedt Incorporated, Alimentix, and the Frestedt Learning Center
Kasey Sands, PhD, RN, CRQE Specialist I, Frestedt Incorporated, and Alimentix

Approved for 1.0 ACRP Contact Hours | Expires November 2, 2025