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Intro
What Details are we
collecting?
How do I register my
IBD Patients?
Who can participate?
What will it entail?
Who will manage the registry?
What about patient consent?
Who will have access to my
Information?
What about patient consent?

  • Section 15 of The National Health Act 61 of 2003 states that no information of a patient may be disclosed unless the patient has consented in writing, or a court has ordered such disclosure, or a law requires it, or where nondisclosure represents a serious threat to public health.


  • Aggregated information being used for the IBD research project will be depersonalised to comply with the relevant sections of the act.


  • Patient consent forms are available online (copy included in your pack). We strongly recommend that all Doctors participating in the IBD research project complete and store a form for every patient.