Good Clinical Practice (GCP) Training Course
This course equips clinical research professionals with practical skills to ensure compliant and efficient heart failure trials under ICH-GCP standards, including SOPs, templates, and inspection readiness.

from 4 to 360h flexible workload
certificate valid in your country
What will I learn?
The Good Clinical Practice (GCP) Training Course provides focused, practical guidance to conduct compliant heart failure trials in the United States. Learn essential ICH-GCP principles, safety reporting, informed consent, data integrity, and documentation standards. Gain ready-to-use SOPs, role-based training activities, inspection preparation steps, and templates that streamline daily tasks and support reliable, audit-ready research.
Elevify advantages
Develop skills
- GCP deviation management: investigate issues quickly and document CAPA like a pro.
- Informed consent mastery: run, document, and fix consent for complex HF trials.
- Drug accountability skills: control IP storage, dispensing, returns, and logs with ease.
- Safety reporting expertise: detect SAEs and submit compliant reports on tight timelines.
- Audit-ready documentation: build TMF, logs, and checklists that pass FDA inspection.
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
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