Good Clinical Practice Course
This course equips professionals with essential skills for conducting compliant and ethical clinical trials, covering ICH-GCP principles, site management, safety reporting, and quality assurance from start to finish.

4 to 360 hours of flexible workload
certificate valid in your country
What Will I Learn?
The Good Clinical Practice Course provides a focused, practical overview of ICH E6(R2) principles, ethics committee and informed consent requirements, protocol design, and site start-up. Learn how to manage documentation, monitoring, audits, and CAPA, while strengthening safety surveillance, SAE reporting, and risk management to support compliant, high-quality clinical trials from initiation to closeout.
Elevify Advantages
Develop Skills
- Apply ICH-GCP and local regulations: run compliant, audit-ready trials fast.
- Design ethical consent: clear ICFs, fair compensation, and strong safeguards.
- Set up high-quality sites: SOPs, delegation logs, and clean source documentation.
- Build robust safety systems: SAE workflows, timelines, and risk mitigation plans.
- Lead monitoring and CAPA: remote visits, root cause analysis, and SOP updates.
Suggested Summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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