The Association of Clinical Research Professionals

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

Pricing With Contact Hours

Member: $15 | Nonmember: $75

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This course is approved for 1.0 ACRP contact hours. Accreditation Details


Pricing Without Contact Hours

Member: $0 | Nonmember: N/A

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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

This course 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 Webinar, attendees should be able to understand and identify:

  1. Understand general considerations for clinical trials
  2. Describe clinical trial development plans
  3. List phases of clinical development

Replay Expires November 2, 2025.