How It Works
Before Your Study Starts
From idea to ethics approval
You tell us about your research question. Our software generates draft documentation: protocol, IRAS application, consent forms, and questionnaires, drawing on patterns from previous successful submissions.
You review, refine, and submit. What usually takes months of administrative work becomes weeks.
Running Your Study
Recruitment and data collection that works for families
Study websites that recruit
Each study gets a public-facing portal where families can learn about the research, check eligibility, and enrol.
Digital consent that's actually readable
Consent forms designed for parents, with age-appropriate assent modules for children. Legally compliant, ethically sound, and not written in legalese.
Questionnaires that reach people
Delivered by SMS or email. No app to download. Personalised reminders to maximise completion rates.
Multimedia when you need it
Collect text, images, audio, or video, securely linked to each participant's record.
Your Data
One source of truth
Everything lives in one place: family-reported data, clinician entries, and information pulled from medical records. Export to SPSS, R, or SAS when you're ready for analysis.
Full audit trails. Role-based access. GCP-compliant.