Description

Enhance your expertise in clinical trials with our comprehensive Good Clinical Practice (GCP) course, now available on our Learning Management System (LMS). This course, align with the ICH GCP R2 and South African GCP guidelines, is an essential educational tool for professionals in the clinical research field. It provides 16 hours of rich instructional content covering the drug discovery and development process, the origins and evolution of GCP, and the ethical considerations in clinical research.

Trainees will delve into the responsibilities of sponsors and investigators, understand the regulatory authority’s role, and learn about the informed consent process. The course also emphasizes the importance of essential documents, source data collection, reporting, and the critical aspects of quality assurance and control.

Upon completion of practical exercises and achieving a minimum score of 80% on the requisite test— with two attempts allowed—participants will earn a Certificate of Completion and 16 Ethics points. Should additional support be needed, a review meeting is offered to ensure comprehension and success.

This GCP certificate, priced at R2950,00, is not only an investment in your professional development but also remains valid for three years, ensuring your credentials stay current in the evolving landscape of health research. Enrol now in our GCP course to secure your spot at the forefront of clinical research excellence.