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
Speakers 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