Basic Full Day
GCP Course
This course is applicable to anyone new to clinical research and persons who have an expired GCP certificate.
-
7 days
Time to complete the course -
3 hours
Video content duration -
2 hours
Open book online tests
New to the clinical research industry?
This comprehensive online course will guide your through all the applicable guidelines that will be of great importance to you in your new environment. 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.
Study at your own pace
You can enroll in this course whenever you want, and study at your own time and pace, but you must complete it within 7 days.
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 for 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.
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.
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.
Carin Coetzee
Carin Coetzee is a Senior Auditor in the FARMOVS Quality Assurance Division. She holds a Master’s degree in Microbiology with more than 10 years’ experience in the clinical research environment. Carin provides guidance to other Divisions as a Subject Matter Expert in GxP standards, industry standards and regulatory requirements. Carin will guide you through the importance of Standard Operating Procedures in clinical research.
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.
Gloria Tsie
Sister Gloria Tsie is a qualified Nurse with more than 8 years’ experience in clinical research. Gloria gained valuable industry experience, before becoming a Clinical Research Coordinator at FARMOVS. She will present the module on Procedures prior to Clinical Trial Execution.
Jolandè Fourie
Jolandé Fourie is a Subject Matter Expert (SME) in ethics and regulatory activities within the clinical trial environment. She holds a MMedSc degree and has 23 years’ experience in clinical research. As the Senior Regulatory Specialist at FARMOVS she has gained ample experience in the module that she will present, namely Ethics and Regulatory Submissions and Approvals.
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.
Estè Vorster
Esté Vorster is a qualified Pharmacist and has 22 years’ experience in clinical research. She holds a Master’s degree in Pharmaceutics and takes the lead as our Responsible Pharmacist on studies and manages the FARMOVS Pharmaceutical Services Division. She oversees all activities around Investigational Product handling and storage. She will share her knowledge in the module on Investigational Products.
Jianine Jonker
Jianine Jonker is a Subject Matter Expert in Quality Management and has led the Quality Management Division for the past 21 years. This group provides support to our operational teams to promote high-quality outcomes for every clinical trial. She holds an MBA and a BSc Honours degree and has the required insight to guide you through the module on Quality Aspects in Clinical Trials.
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.
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