ICH E6 (R2) Good Clinical Practice

ICH E6 Thumbnail.png
ICH E6 Thumbnail.png

ICH E6 (R2) Good Clinical Practice

from 189.00

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This Good Clinical Practice (GCP) course covers the requirements of GCP for clinical trials found in ICH E6 (R2) related to the role of the sponsor and investigator. The required activities related to the sponsor and investigator GCP roles and responsibilities are presented with case studies to reinforce key concepts and emphasize critical activities.

This ICH E6 (R2) GCP Training meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma as necessary to enable mutual recognition of GCP training among trial sponsors. 

Course Length: 75 minutes


  • Unlimited access to the content for 30 consecutive days during a 90-day period from your initial day of purchase.

  • Certificate of completion

  • Case Studies

  • Post-Assesment

  • Knowledge Checks


  1. Apply critical thinking techniques for effective implementation of the global Good Clinical Practice Guideline, ICH E6(R2) guideline

  2. Discover how the ICH global guideline affects your role

  3. Reflect on challenges and opportunities in implementing Good Clinical Practice or the GCP Guideline

  4. Identify practical applications of the guideline in your work


All clinical research personnel