Good Clinical Practice

• Module 1 - Introduction
• Module 2 - Key Changes brought about by ICH GCP E6 R2 Addendum
• Module 3 - History and Principles of ICH-GCP
• Module 4 - Informed Consent Process, Documentation
• Module 5 - Roles and Responsibilities according to ICH-GCP
• Module 6 - Adverse and Serious Adverse Events
• Module 7 - Essential Documents
• Module 8 - Drug Compliance and Accountability
• Module 9 - Monitoring, Auditing and Inspections

This training is also available as a corporate solution, which allows professionals with administrative functions, such as R&D, Training, QA, Clinical Operation, HR Managers, to manage and monitor the whole learning process/curve:

• licences and access management
• performance statistics and outcomes
• certificate management
• reports

The GCP training is also offered in the form of face-to-face training, where experts from our International Network of Trainers come to you; additional content customisations are available upon request.