Good Clinical Practice (GCP) Course
This course equips researchers with essential GCP knowledge tailored to Brazilian regulations, covering ethics submissions, consent processes, safety management, and data protection for compliant clinical studies.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
The Good Clinical Practice (GCP) Course provides a straightforward, practical guide to conducting compliant and ethical studies in Brazil. You will learn about CEP/CONEP submissions, study conduct based on GCP, informed consent for participants with low literacy, management of adverse events (AE) and serious adverse events (SAE), confidentiality aligned with LGPD, and fair recruitment and payments, ensuring your research adheres to Brazilian and international standards confidently and efficiently.
Elevify advantages
Develop skills
- Mastery of GCP ethics: apply Brazilian and ICH-GCP guidelines in everyday research activities.
- CEP/CONEP submissions: prepare, submit, and monitor ethics packages without any hold-ups.
- Informed consent design: develop simple forms and verbal explanations quickly for low-literacy groups.
- AE/SAE safety processes: assess, record, and report incidents accurately and promptly.
- Data integrity in clinics: safeguard privacy, source documents, and CRFs to meet audit standards.
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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