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ABC of Quality Control

Running a clinical trial is a complex and detailed process. Maintaining accurate records and quality data throughout a clinical trial is a continual, dynamic process.

Trial requirements are carefully prescribed in detailed documents such as the protocol, the ICH and SA GCP guidelines, data management plan and the project plan.

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This practical course will equip clinical research site personnel with the relevant knowledge and tools to ensure successful study conduct from start to finish, in preparation for monitoring audits and site inspections.

Available as classroom training
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Classroom - R3,850 (VAT inclusive).  

For group discounts, please contact us at

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The classroom training is two full days (from 08h30 to 16h00).

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Target Audience

Clinical research personnel such as investigators, study coordinators, and project managers with a valid GCP certificate and preferably some work experience in the clinical research field.

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Delegates are required to complete a final assessment with at least 70% accuracy.

Upon successful completion of the course, the delegate will be given access to the Certificate of Completion.

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CPD Points

CPD points will be issued with the certificate of completion.

(8 CPD points | 2 Ethics points).

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In-house Training

In-house training will be considered, subject to viability.