Good Clinical Practice Course
Master Good Clinical Practice to run safe, compliant clinical trials. Learn ethics, informed consent, protocol design, safety reporting, monitoring, CAPA, and documentation so you can protect participants and meet global regulatory standards.

from 4 to 360h flexible workload
certificate valid in your country
What will I learn?
The Good Clinical Practice Course delivers 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 workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
FAQs
Who is Elevify? How does it work?
Do the courses have certificates?
Are the courses free?
What is the course workload?
What are the courses like?
How do the courses work?
What is the duration of the courses?
What is the cost or price of the courses?
What is an EAD or online course and how does it work?
Course in PDF