Good Clinical Practices Course
This course equips learners with essential knowledge and practical skills for conducting ethical and compliant clinical trials under Good Clinical Practices (GCP) standards, covering key areas like consent, data management, safety, and protocol adherence.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
The Good Clinical Practices Course provides practical, step-by-step guidance to conduct compliant and ethical clinical trials with confidence. You will learn about informed consent and participant rights, core GCP principles, data integrity, safety reporting, managing protocol deviations, and efficient clinic workflows. Develop skills in creating audit-ready documentation and understanding global regulations to ensure your studies remain accurate, transparent, and prepared for inspections.
Elevify advantages
Develop skills
- Master informed consent by applying GCP, HIPAA/GDPR, and participant rights quickly.
- Ensure GCP-compliant data through ALCOA+ source notes, eCRFs, and audit-ready files.
- Handle adverse events and serious adverse events by classifying, documenting, and reporting safety events on time.
- Manage protocol deviations by performing root cause analysis, CAPA, and timely reporting.
- Run trial visits in the clinic using SOP-driven workflows, logs, and monitoring readiness.
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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