The Office of Research Integrity (ORI) at UCT is responsible for overseeing ethical research conduct, ensuring compliance with biosafety standards, and promoting research integrity throughout the university. This page outlines the key components of ethics, biosafety, and research integrity supported at UCT.

Ethics and Biosafety

Research conducted at UCT must adhere to the UCT Policy for Responsible Conduct of Research. Oversight is provided by ethics, animal ethics, and biosafety committees operating at both the Senate and faculty levels. These committees develop and implement ethical policies, ensuring compliance in research involving human participants, animals, and potentially hazardous biological agents.

Use this guide as a quick reference to understand the research ethics landscape at UCT:

Process guide: UCT Ethics and Biosafety Committees

All projects involving human participants, biological materials, animals, or potentially hazardous biological agents (pHBAs) require prior approval from the relevant ethics or biosafety committee. 

Detailed steps for determining and obtaining the necessary approvals are outlined below.

Determining the need for ethics approval

Projects involving human participants are reviewed by the relevant Faculty Research Ethics Committee (REC), or the Inter-Faculty Human Research Ethics Committee (IFHREC) for inter-faculty or trans-disciplinary health-related research. A pre-screening questionnaire (PSQ) on UCT eRA assists in determining whether approval is required and identifies considerations relating to the Protection of Personal Information Act.

Research using human or animal biological materials, plant-based research, or potentially hazardous biological agents requires Faculty Biosafety Committee approval, with some cases referred to the Institutional Biosafety Ethics Committee. Guidance is available in the Institutional Biosafety Policy.

Animal research projects require review from Faculty Animal Ethics Committees, and in some cases, may also require a Section 20 permit from the Department of Agriculture and procedures authorisation from the South African Veterinary Council. Biosafety approval may also be necessary for certain projects.

Research involving anonymised third-party data (secondary data) may require approval if identifiable elements are accessible. Relevant Faculty Ethics Committees provide advice in such cases.

Each faculty has specific ethics and biosafety procedures.

For information about the research ethics of individual faculties, see these links:

Projects requiring health-related ethics approval outside the Faculty of Health Sciences or involving inter-faculty collaboration are reviewed by the Inter-Faculty Human Research Ethics Committee (IFHREC).

If a pre-screening questionnaire (PSQ) determines that ethics approval is not required, exemption letters are provided via UCT eRA.

If ethics approval is required, the following steps apply

1. Submitting an ethics application

Applications requiring ethics or biosafety approval must be submitted via the UCT eRA system to the appropriate committee. Submission instructions specific to each faculty are available on their respective webpages.

2. Committee review and outcome

Ethics applications are reviewed by the relevant committee, and outcomes are issued through UCT eRA:

  • Approved/Authorised
  • Approved/Authorised with conditions
  • Not Approved/Authorised

Outcome letters can be downloaded via UCT eRA. Assistance is available through the guide Ethics Management – Generating an outcome letter.

Appeals addressing procedural errors or conflicts of interest may be submitted to the following bodies:

  • Senate Ethics in Research Committee
  • Senate Animal Ethics Committee
  • Institutional Biosafety Ethics Committee

Appeals are considered in exceptional cases and should only be initiated once all other avenues have been exhausted.

Research Integrity

Research integrity at UCT is underpinned by honest and verifiable methods, adherence to domain-specific standards, and compliance with institutional and professional regulations. It focuses on translating research into meaningful outcomes while maintaining public trust.

The responsible conduct of research (RCR) is a cornerstone of integrity, fostering accountability and professionalism across disciplines. RCR training equips researchers to address ethical challenges, comply with regulations, and adopt best practices in areas such as data management, authorship, peer review, and the prevention of misconduct (e.g., plagiarism, fabrication, and falsification). It also supports the ethical management of human and animal subjects in research.

International research funders increasingly require evidence of RCR training. UCT offers a range of training and education opportunities, including:

  • Asynchronous online learning through SuccessFactors (search “integrity” after logging in)
  • In-person workshops and seminars, advertised via the research announcement newsletter or in collaboration with the ERP and OPGS platforms.

Customised workshops for departments or specific enquiries can be directed to the Office of Research Integrity (ORI). 

Advice and Support

Guidance on research ethics, integrity and best practices is available through the Office of Research Integrity (ORI). See also our Research Integrity section for details.

Research ethics committees (RECs)

The responsible conduct of research at UCT is supported through university-wide and faculty-specific policies, senate-level committees, and faculty-level research ethics committees (RECs):

  • The RECs take responsibility for the review and oversight of research projects that engage with research participants through interactions and/or interventions, and/or use individually identifiable data about living individuals.
  • Their work is shaped by core principles of justice, beneficence, and respect.
  • RECs typically require detailed protocol information relating to:
    • the reasonableness and minimisation of risks  
    • the balancing of risks and benefits associated with participation
    • assurance as to the equitable representation of persons, and
    • support for the voluntarism associated with ethics research.
  • RECs also undertake special scrutiny of research that engages with vulnerable populations including, among others:
    • children
    • pregnant women and foetuses
    • prisoners
    • migrants, and
    • people who are cognitively impaired.
  • Faculty-level animal ethics committees (AECs) provide similar oversight for animal welfare and well-being in research projects ranging from laboratory research to wildlife-field studies.

Statement by the Senate Ethics in Research Committee on the review of Health Research

  1. All research conducted at the University of Cape Town (UCT), whether by academic or PASS staff members or students (both undergraduate and postgraduate), and post-doctoral fellows (hereafter: UCT community), which meets the definition of health research, must undergo review by a UCT research ethics committee (REC) registered with the National Health Research Ethics Council (NHREC).
  2. The review of health research must be done before any research activities (such as interviews or data collection) commence. Retrospective approval will not be granted.
  3. No health research may be conducted until written approval from an NHREC registered REC has been received.

UCT has 2 committees registered with the NHREC able to review Health Research:

  1. The Faculty of Health Sciences Human Research Ethics Committee (HREC), based in the Faculty of Health Sciences (FHS). Any research conducted by staff and students based in the FHS must be reviewed and approved by the HREC. Further information regarding their processes is available on their website, or via email to: hrec-enquiries@uct.ac.za.
  2. The Inter-Faculty Human Research Ethics Committee (IFHREC), serviced by the Office of Research Integrity. All staff and students who plan to conduct health research (as per the definition) and who are based in the Faculties of Commerce, Engineering and the Built Environment, Humanities and Law; the Centre for Higher Education and Development and the Graduate School of Business must submit their applications to the IFHREC. This includes staff in PASS departments who may be conducting health research. Further information regarding their processes is available on their website, or via email to: ifhrec.enquiries@uct.ac.za.

If there is in any doubt as to whether research constitutes health research, then a researcher must use the screening tool developed by the EiRC to determine which committee is most appropriate to review the proposed research. This tool may be accessed here.

  Please note: this tool is currently being used as a pilot. If you have feedback or comments please send them to the Office of Research Integrity

Guidelines and Standards

UCT Guidance

UCT Guideline for Risk-Based Ethical Review of Research (Human Participants)

Guidelines and recommendations for the use of generative artificial intelligence (AI) tools in research

Recommendations: Standard criteria for inclusion in research invitations

Statement by the Senate Ethics in Research Committee on review of Health Research

 

South African National Standards and Guidelines

South African Ethics in Health Research Guidelines: Principles, Processes and Structures, 2024, 3rd ed. (NDoH 2024)

SANS10386:2021 The South African National Standard for the Care and Use of Animals for Scientific Purposes

  PLEASE NOTE: The SANS10386:2021 is a restricted access document. It is only available to UCT staff and students and will require you to sign-in using your institutional credentials to view it. You cannot download or print the document. 

 

Senate-level research ethics committees (RECs)

Human Subjects

 

  • Inter-Faculty Human Research Ethics Committee (IFHREC)
  • Visit website for Terms of Reference and other supporting information

 

Animal Subjects

 

Faculty-level research ethics committees (RECs)

Human subjects

 

Animal ethics

 

 

For more information on research integrity contact the Office of Research Integrity