Get your ICH GCP Certificate today!
Ensure compliance, quality, and ethical integrity in clinical research with our in-depth ICH GCP training.
This course meets TransCelerate BioPharma Criteria to enable mutual recognition!
This course covers the content of ICH GCP E6 Revision 3:
- Key principles of Good Clinical Practice.
- Roles and responsibilities of sponsors, investigators, IRBs and monitors.
- Safety Reporting and Informed Consent
- Data Governance and Essential Records
Join today and get your certficate!
Gain immediate access for just €75, easily payable via PayPal, or contact us for alternative payment options. Learn at your own pace, enhance your expertise, and ensure your trials meet the highest global standards.
Welcome to "Unveiled ICH GCP R3: Essential Updates and Practical Steps for Implementation!" Discover the major updates in the Good Clinical Practice Guideline Revision 3, and their impact on the conduct of clinical studies. This webinar offers a concise overview of the key changes; with practical guidance to help integrate them into your processes!
