The process for submitting a new staff research protocol for approval by the DRC and HREC is described here.
This is applicable to all staff in the SPH.
You can download the pdf here and please review the SPH DRC pointers for new protocol submissions
NEW R1 internal review form - download here
The process for submitting a new degree student research protocol for approval by the DRC and HREC is described here.
This applicable to PhD and Masters students.
You can download the pdf here and please review the SPH DRC pointers for new protocol submissions
You can download the SPH and DRC ethics application submission dates here
Research Ethics Training Requirement – What You Need to Know
In line with the current National Human Research Ethics guidelines, the UCT Faculty of Health Sciences Human Research Ethics Committee (HREC) has introduced a mandatory ethics training requirement for all investigators conducting research with human participants, their data, or samples at UCT. Note that this is not specific to UCT and is a requirement for all human subjects research in South Africa.
1. Who must complete ethics training?
Everyone with direct or indirect interaction with human participants or their data or samples
All staff and researchers (including principal investigators, co-investigators, supervisors, research coordinators, fieldworkers, study staff, research assistants)
Postdoctoral fellows
All students conducting research (undergraduate, postgraduate, honours, master’s, PhD)
- Non-UCT collaborators
2. What research does this apply to?
All types of health research: quantitative, qualitative, clinical trials, case reports, audits, database research, systematic/scoping reviews, folder reviews etc.
3. When does this requirement apply?
- Revised effective date is 1 July 2026, following which the HREC will not accept new protocol submissions or annual progress reports without proof of valid research ethics training.
- Certification must be renewed every 3 years.
4. What do you need to?
Training must be completed before submitting new HREC applications or annual progress reports.
New protocol applications:
These must be submitted to the DRC as usual. All new protocols that will reach HREC on or after 1 July 2026 must include training certificates (obtained within the past 3 years) for all investigators
Annual progress reports:
These do not come through the DRC but are submitted directly to HREC. All progress reports submitted from 1 July 2026 must include training certificates (obtained within the past 3 years) for all investigators
5. Plan to avoid delays with your applications
Complete your training or confirm that your current training is acceptable and valid.
Certification obtained within the past 3 years will be recognised if valid as of 1 July 2026.
Ensure that all students, investigators and study staff on protocols for which you are PI have completed the relevant training.
6. What training counts?
Preferred UCT training:
Responsible Conduct of Research (RCR) - Available on the SuccessFactors Learning Platform (free for UCT staff, postdocs, master’s, and doctoral students). http://www.successfactors.uct.ac.za/
Highly recommend completing all modules but the HREC required modules are:
Module 4: Research Involving Human Participants
Module 5: Managing and Sharing Human Research Data
Other accepted training:
- TRREE (Training and Resources in Research Ethics Evaluation) https://elearning.trree.org/
Online course (recommended for undergraduate and honours students, or anyone without SuccessFactors access). Required modules: 1-3 - TCPS 2 (Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans) – https://tcps2core.ca/welcome
- CITI Program courses on Human Subjects Protection: https://about.citiprogram.org/series/human-subjects-research-hsr/
- WHO Research Ethics Online Training: https://globalhealthtrainingcentre.tghn.org/research-ethics-online-training-v2/
Note for non-UCT investigators: Collaborators who have a valid ethics training within the past 3 years may submit this for HREC review. The HREC will accept alternative training courses if they include both an assessment and certification of training. Those who have not completed ethics training in the past 3 years should complete one of the alternative courses listed above.
7. Additional training required for clinical trials:
Clinical trials researchers must also maintain valid SA GCP (Good Clinical Practice) certification.
8. Support and queries
- Technical issues with SuccessFactors modules:
Contact the Office of Research Integrity (research.integrity@uct.ac.za)
- Questions about HREC requirements:
Review the HREC website for the latest details:
https://health.uct.ac.za/home/human-research-ethics
Contact hrec-enquiries@uct.ac.za
- Process questions:
Review the DRC website for the latest details:
https://health.uct.ac.za/school-public-health/research/departmental-research-committee
Contact the SPH DRC: sph-drcethics@uct.ac.za