The clinical research lifecycle, one phase at a time.

Designing the study on paper. Hypothesis → literature search → endpoints → R-powered power analysis → CONSORT/STROBE-bound methods → Statistical Analysis Plan → protocol draft. Supported today for parallel-group RCTs and cross-sectional studies. Multi-arm, crossover, cluster, and observational cohort designs are on the roadmap — tell us what you would use first.

Getting the study ready to run. Case Report Form auto-generated from your locked endpoints. Participant Information Leaflet rewritten in patient-friendly language. Informed consent form. Randomisation plan (block, stratified, simple) where applicable. Trial registry submission preparation. Targeted at clinician-led research that needs ethics submission and site readiness without a full CRO.

Running the study. Live data collection on the Case Report Form you designed in Prepare, integrated with SynapseCPT. Screening logs, enrolment tracking, visit scheduling, adverse-event capture, and site monitoring. The data layer connects forward into Publish so analysis runs on the actual captured dataset rather than a separate export.

Turning collected data into a manuscript. The locked Statistical Analysis Plan runs automatically against the captured dataset, with deviations from the pre-specified plan surfaced explicitly. Flow diagram where applicable, Table 1, results section drafted from real numbers, discussion grounded in the project's evidence library, and registry results posting.