Submit de-identified patient observations using cryptographic tokens. Organize peer-reviewable studies. Export CONSORT-ready data with AI assistance — no IRB headaches, no IT department, no cost.
Academic EDC systems require institutional access, IT setup, and IRB approval even for retrospective chart reviews.
Physicians have clinically rich data that could advance science — but HIPAA compliance makes sharing prohibitively complex.
Promising observations stay in filing cabinets because there’s no structured, exportable, checklist-compliant format.
How it works
No data governance training required. Your patient identifiers never leave your browser.
Type your local chart number. hyJournal creates a SHA-256 hash in your browser. Only the token is submitted — never the patient ID.
SHA-256 · Client-side · IrreversibleFill structured forms: ICD-10 diagnoses, RxNorm-normalized drugs, MedDRA-coded AEs, biomarkers, and validated outcome scales.
CRF-style · Specialty templatesCreate study arms, pre-register your protocol with a cryptographic hash, and invite co-investigators.
Pre-registration · K-anonymity gateRun AI statistics, complete CONSORT/STROBE checklists, generate a manuscript skeleton, and export in 6 formats.
ICMJE compliant · SDTM · FHIR R4Privacy architecture
Implements HIPAA Safe Harbor (45 CFR §164.514(b)(2)) — all 18 identifiers suppressed.
Platform features
25 items for RCTs, 22 for observational. Each evaluated against your data with ✓/⚠/✗ status and fix guidance.
Peer-review readyLock your protocol before data collection. SHA-256 hash + UTC timestamp — equivalent to ClinicalTrials.gov for independent studies.
Anti-HARKingNormality checks, test selection, multiplicity correction, Clinical Scenario Evaluation power analysis. No R or Python required.
CDISC-readyeGFR, MELD, SOFA, APACHE-II, CHADS₂-VASc, ASCVD, PHQ-9, GAD-7, DAS-28, KOOS, CDAI, NIHSS, MMSE, Framingham CHD, Wells DVT.
Evidence-basedReal-time canonical drug name + RxCUI code. Prevents spelling variation across submitters. Pulls expected AEs from OpenFDA.
RxNorm + OpenFDAGenerate Intro/Methods/Results skeleton. Reviewer agent verifies PMIDs are real and statistics match your dataset.
Claude-poweredGenerate a complete IRB narrative from your protocol including the de-identification method, risk/benefit, and data protection sections.
IRB-readyScreening / Baseline / Week 4 / Month 6 / EOS windows with tolerance bands. Track dropout, LTFU, and protocol deviations.
EDC-styleBox + violin, Kaplan-Meier, forest plots, CONSORT flowcharts, Bland-Altman, heatmaps at 300 DPI JAMA style.
JAMA styleExport formats
Every export is designed to slot directly into the workflow of the journal, regulator, or EHR system receiving it.
Specialty templates
Journal compatibility
ICMJE requires a data sharing statement for all clinical trial manuscripts. hyJournal auto-generates it.
Get started today
Free forever for independent researchers. No credit card. No IRB approval needed for observational studies.
hyJournal does not store Protected Health Information (PHI). All patient records are cryptographically tokenized client-side using SHA-256 before transmission.