Good Clinical Practices Course
Master Good Clinical Practice in real hospital settings. Learn informed consent, data integrity, AE reporting, protocol compliance, and ethics so you can protect patients, satisfy regulators, and run safer, audit‑ready clinical trials.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
The Good Clinical Practices Course gives you practical, step‑by‑step guidance to run compliant, ethical trials with confidence. Learn informed consent and participant rights, core GCP principles, data integrity, safety reporting, protocol deviation management, and efficient clinic workflows. Build audit‑ready documentation skills and understand global regulations so your studies stay accurate, transparent, and inspection‑ready.
Elevify advantages
Develop skills
- Master informed consent: apply GCP, HIPAA/GDPR, and participant rights fast.
- Ensure GCP-compliant data: ALCOA+ source notes, eCRFs, and audit-ready files.
- Handle AEs and SAEs: classify, document, and report safety events on time.
- Manage protocol deviations: perform root cause, CAPA, and timely reporting.
- Run trial visits in clinic: 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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