Refresher GCP Course
This course is for persons who have already completed the Basic GCP course, and need to renew it before it expires. You can sign up for the refresher course, every 3 years.
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7 days
Time to complete course -
2.5 hours
Video content duration -
2 hours
Open book
online tests
Certificate about to expire soon?
This refresher course will guide your through all the applicable guidelines, focusing on the basics and important updates. The course adheres to regulatory authority requirements and international Good Clinical Practice guidelines.
What's included in this online course?
A detailed guide
Our presenters will share the main points, essential to regulatory compliance.
Flexible Completion
You can enroll in this course whenever you want, and you will have 7 days to complete this workshop.
Unique learning experience
Multiple presenters will share their knowledge with you, each an expert in their field. Every module is followed by a short quiz to prepare you for the final assessment.
Get to know us
Presenters in this course
Charmaine van der Walt
Charmaine van der Walt boasts with 26 years’ experience as a Quality Assurance Auditor in clinical research. She has an MSc Quality Management degree and leads the FARMOVS Quality Assurance Division as a Subject Matter Expert. Charmaine gained valuable experience as a qualified Nurse before joining FARMOVS. She will present the module on Ethical and Regulatory Environment for Clinical Trials.
Dr Muhammad Rajah
Dr Muhammad Rajah is a Clinical Research Physician at FARMOVS. He holds a MBChB degree and has been directly involved in the clinical care of patients since 2019. He has gained experience as both a Principal and Sub-Investigator for a variety of clinical trials. He will be providing an overview of drug development and the pre-clinical trial process, in addition to the requirements for the clinical trial process.
Annika Möller
Annika Möller is a registered Dietitian who joined the FARMOVS Project Management Division mid- 2022. As a Project Manager, Annika is the main point of communication between FARMOVS and study Sponsors and ensures that communication and all the administrative components run smoothly throughout the pre-clinical, clinical and post-clinical trial phases. She will present the modules on Essential Documents and Clinical Trial Process Introduction and Procedures before Clinical Execution.
Henk DeVasch
Henk de Vasch gained valuable healthcare industry experience as a qualified Orthopaedic Nurse before he joined FARMOVS in 2015. As a Clinical Research Coordinator, he is responsible for the clinical execution, coordination, and management of clinical studies. He will present the modules on Source Data and CRFs and Procedures during Clinical Execution.
Jean Tola
Jean Tola is a Subject Matter Expert (SME) in Data Management and Quality Assurance. She joined the FARMOVS Quality Assurance Division in 2020, as a Quality Assurance Auditor, where she provides guidance as an SME in GxP standards, industry standards and regulatory requirements. She will be presenting the modules on Post Clinical Trial Data Handling and Post Clinical Trial Procedures.
Dr Edrich Krantz
Dr Edrich Krantz is a Senior Clinical Research Physician at FARMOVS. His journey in clinical research began in 2008. He has a MBChB degree and was a General Practitioner in private practice for 25 years before joining FARMOVS. He will present the modules on Investigator Responsibilities and Adverse Events in Clinical Trials.
Dr Reinard McPherson
Dr Reinard McPherson, a proud University of the Free State MBChB graduate, has 18 years’ experience in clinical research within multiple portfolios. As Chief Medical Officer at FARMOVS, he is responsible for the clinical research unit in addition to ancillary scientific FARMOVS services, and business development activities. He will present the modules on Safety Monitoring, Recording and Reporting, as well as Informed Consent and Vulnerable Populations.
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