Good Clinical Practices Course
Gain expertise in Good Clinical Practice for hospital environments. Master informed consent, data integrity, adverse event reporting, protocol adherence, and ethical standards to safeguard patients, meet regulatory needs, and conduct secure, inspection-ready clinical trials in line with global rules.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This Good Clinical Practices Course offers clear, practical steps to manage ethical and compliant clinical trials confidently. Cover informed consent, participant rights, key GCP principles, data integrity, safety reporting, protocol deviations, and streamlined clinic operations. Develop skills for audit-proof records and grasp international regulations to ensure studies remain precise, open, and ready for inspections.
Elevify advantages
Develop skills
- Master informed consent processes using GCP, HIPAA/GDPR, and participant rights principles.
- Ensure data complies with GCP through ALCOA+ source notes, eCRFs, and audit-ready records.
- Handle adverse events and serious adverse events by classifying, documenting, and reporting promptly.
- Manage protocol deviations with root cause analysis, CAPA plans, and timely reporting.
- Conduct efficient trial visits in clinics using SOP-driven workflows, logs, and monitoring preparation.
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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