Practical templates, checklists, and guidance for preregistration, preprints, data sharing, consent, and publishing reproducible research.
Interactive template to preregister hypotheses, outcomes, analysis plans, ethics and data-sharing details, and to assess preprint readiness. Save structured responses, link to registries and preprint servers, and produce a clear readiness score.
Interactive preregistration template and checklist to support transparent study design, reduce analytic flexibility, and capture commitments for preprints, data, and code sharing.
A practical pack of IRB-friendly consent language examples, three adaptable template consent forms, a concise participant information sheet, an IRB submission checklist, data-sharing and privacy clauses, and a dual-use / biosafety risk checklist to consider during protocol design. Includes usage guidance and adaptation notes for common study types (survey, secondary data, clinical/biobanking).