- Introduction & Principles of ICH-GCP
- Informed Consent
- Ethics
- Responsibilities of Investigator
- Responsibilities of Sponsor
- Clinical Trial Protocol
- Investigator Brochure
- Essential Documents
All our Online GCP Training material includes all the changes/amendments proposed in the EU Directive 2005/28/EC and is in line with current regulations.
All trainees receive free access to the course content, resources and useful documents for 6 months after account activation