Good Laboratory Practice (GLP) Course

Explore GLP clinical trials in our specialized course designed for professionals in clinical and laboratory research.

  • 7 Day

    Time to complete the course

  • 2 Hours

    Video duration

  • 1 Hour

    Online Test
    Course Overview
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    What We Offer

    What's included in this online course?

    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 

    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 the presenters

    Course Presenters

    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.

    Amaria Saayman

    Amaria Saayman is the Laboratory Director since 2021. She started her career as a Bioanalytical Scientist in 2008 after completing a BSc Hons degree in Biochemistry and worked for more than 15 years in analytical- and molecular research laboratories. She is currently responsible for the overall management of the Bioanalytical Services Division to ensure the optimal functioning of the laboratories. She will be presenting the module on the Overview of Good Laboratory Practice.

    Zintle Gwane

    Zintle Gwane is a clinical research professional who holds a BSc Honours degree in Chemistry and has two years of experience in clinical research working as a Data Bioanalyst. Her day-to-day duties include processing and statistically evaluating data that is generated during validation and bioanalytical phases of studies as well as compilation of reports. She will be presenting the module on Why was GLP implemented.

    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.

    Jéan-Wayne Clements

    Jéan-Wayne Clements is a clinical research professional who holds Bachelor of Science Honours in Environmental Sciences with Biodiversity and Conservation Ecology and has two years of experience in clinical research working as a Data Bioanalyst. His day-to-day duties include development and practical execution of analytical methods including quantitative or qualitative analysis of exogenous or endogenous compounds in biological fluids or other materials. He will be presenting the module on Implementation of GLP.

    Andrea Snijman

    Andrea Snijman is a Data Bioanalyst for the past 2 years. She holds a M.Sc Organic Chemistry and responsible for the processing and interpretation of analytical data accumulated during the validation and production phases of studies, the collation of processed data and the compilation of the validation and bioanalytical reports. She will be presenting the module on the Purpose of GLP.

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