Multicentre ortho studies, EDC, ePROMs and audit trail
Run multicentre orthopaedic studies with confidence. EDC, ePROMs, audit trail, GDPR, and investigator workflow in one place — built for the way surgeons actually run registries and cohorts.

Clinical research lives or dies on the unglamorous bits: audit, access control, export fidelity, and whether the form submits when the wi-fi is patchy in a side room. We start there.
Browse open studies and apply to join as a site investigator, research fellow, or manuscript author.
Open →Got a research question? Submit a proposal — the steering committee reviews monthly.
Open →Browse every investigator on the platform. Filter by institution, specialty, or study.
Open →
Electronic data capture designed for investigator-led orthopaedic registries and prospective cohorts — not a rebadged generic form tool.
KOOS, HOOS, DASH, Oxford scores and EQ-5D, delivered by secure link and surfaced alongside clinician-entered data on one timeline.
Every change on every field is timestamped and attributable, with old and new values preserved at the database trigger level.
Row-level security, per-field access scoping, column-level encryption for direct identifiers, and per-subject export. UK and EU hosting.
Delegation logs, site activation, training records, and study-scoped RBAC — the admin scaffolding real multicentre studies need.
Long and wide CSV, REDCap-compatible dictionaries, and CDISC ODM-XML — so data lands in your statistician's tool of choice.
Define your case report forms in a declarative schema, add sites, invite collaborators from the OrthoGlobe member directory, and start capturing data. No IT procurement cycle.
Run a registry or prospective cohort without building the infrastructure first — forms, auditability, exports come in the box.
A lightweight investigator workflow with delegation logs, training records, and the paperwork a monitor actually looks at.
ePROM links, visit schedules, and query resolution without emailing spreadsheets between sites.
A browseable directory of active and planned OrthoGlobe collaborative studies with phase, eligibility, sites, investigators, and protocol documents — plus an EDC preview with visit-based forms. Submissions open once membership review is complete.
Vetted OrthoGlobe members can propose studies for review. Approved protocols get a study page, an EDC instance, and collaborator invites across the network.
ALCOA-C audit trail at the database-trigger level, row-level access control, per-field encryption for direct identifiers, and exportable audit logs for monitors and regulators.
UK and EU hosting with GDPR-first defaults. Country-scoped hosting is available for protocols with cross-border data restrictions.
The collaborative runs investigator-led orthopaedic studies under a single brand, with shared infrastructure and a pre-vetted member base.
Investigator-led EDC for multicentre orthopaedic studies. Membership required to enrol as a site PI or sub-investigator.