Draft your MMed protocol, thesis synopsis & HREC submission for HPCSA registration

For postgraduate medical registrars at UCT, Stellenbosch, Wits, and all SA universities. Generate structured draft outlines (headings + guidance) aligned with your institution’s IRB/HREC requirements and Form 57 MED certification.

MMed Research Protocol

UCT FHS015 format, design, sampling, inclusion/exclusion, variables, data collection, resource-limited setting framing.

Thesis Synopsis / Proposal

Background, rationale, aims & objectives, research question, outcomes, supervisor review checklist.

HREC/IRB Submission

Ethics application templates, consent forms (English/Afrikaans/Xhosa), DRC submission guidance.

✓ South Africa-Specific Formats:

UCT Form FHS015 — Complete protocol structure with HREC submission requirements
Stellenbosch / Wits / Other SA Universities — IRB application guidance & supervisor review templates
HPCSA Form 57 MED — Research component certification for specialist registration
Terminology — Registrar (not resident), Supervisor (not guide), IRB/HREC (not IEC), resource-limited/LMIC context

Academic Integrity Notice: This website provides reference-only drafts, templates, and outlines. You must rewrite in your own words, add appropriate citations, verify accuracy, and obtain supervisor/departmental review. Do not submit AI output as-is or represent it as your independent original work.

SA-Specific Research Sections & Keywords

HPCSA research requirement Form 57 MED UCT FHS015 MMed protocol South Africa registrar research protocol MMed thesis synopsis HREC submission IRB application DRC approval Stellenbosch MMed Wits registrar research UCT research protocol study methodology LMIC resource-limited setting aims and objectives literature review outline sample size calculation statistical analysis plan SPSS analysis ethics application template consent form English Afrikaans Xhosa retrospective study protocol cross-sectional study cohort study protocol supervisor approval checklist

These keywords reflect SA university requirements. Output remains reference-only and requires full rewriting and supervisor review.

Generate your draft

Create a structured outline for your MMed protocol / thesis synopsis (reference-only) aligned with HPCSA requirements.

Generate Draft Protocol

R 1,500 ZAR • 24-hour delivery
Reference-only draft. Rewrite fully, verify all details, add citations, and get supervisor approval before submission.

What you’ll receive

Protocol/synopsis section headings matching your university’s format (UCT FHS015, Stellenbosch, Wits)
Methods framework (design, sampling, variables, resource-limited setting framing)
HREC/IRB submission checklist & ethics application guidance
Consent form templates (English/Afrikaans/Xhosa references)
Stats plan guidance (variable list, test selection, reporting)
Supervisor review checklist
Editable DOCX output you can refine

What we do NOT do

No “ready-to-submit” protocols or theses
No guarantees of HREC/DDB approval or publication
No encouragement of plagiarism or academic misconduct
No data analysis or statistical execution

How it works

Enter your topic, setting (hospital/unit), and study type (retrospective, cross-sectional, cohort, etc.).
Specify your university (UCT, Stellenbosch, Wits, other) and department for format alignment.
Select modules: protocol (FHS015 or standard), synopsis/proposal, HREC/IRB submission guidance, stats plan, consent forms.
Receive a structured draft outline and prompts aligned with SA university requirements and HPCSA Form 57 MED.
Rewrite, verify facts, cite sources, and review with your supervisor before DRC/HREC submission.

Frequently Asked Questions

Can I submit the AI output as-is to my DRC/HREC?

No. You must rewrite completely in your own words, verify all medical/scientific accuracy, add proper citations, and obtain supervisor approval before any institutional submission.

Will this guarantee HREC approval or HPCSA registration?

No. This is drafting support only. Approval depends on your supervisor, departmental research committee (DRC), faculty HREC, and compliance with institutional policies.

Do you support UCT Form FHS015 specifically?

Yes. We provide structured outlines matching UCT FHS015 requirements, Stellenbosch formats, Wits guidelines, and general SA university HREC submission standards.

What study types do you support?

Retrospective audits, cross-sectional studies, cohort studies, case-control studies, clinical trials (Phase I-IV), systematic reviews, qualitative research, and mixed-methods designs.

Do you provide consent forms in Afrikaans and Xhosa?

We provide English consent form templates with notes on translation requirements per HREC guidelines. Professional translation to Afrikaans/Xhosa is the registrar’s responsibility.

How does pricing work for international orders?

SA registrars pay R3,000 ZAR (approx. ₹13,000 INR or $50-60 USD). Payment via international card or bank transfer. 24-hour delivery after payment confirmation.