Clinical investigation capture

Proportionate study data capture

ePRO, site forms, consent, and audit trails - without a full CTMS.
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Patients

863

9 reporting clinics

6-month improvement

31

Mean outcome score

Follow-up complete

95%

Across due timepoints

Safety flags

4

Awaiting review

Patient Reported Outcomes

Pain, stiffness, and function · Lower is better · Mean score for 863 patients · 31 point improvement

TimingBaseline
Date12 Jan 2026
Total60/96
Pain13/20
Stiffness5/8
Function42/68

Patients by clinic

Enrolment in the selected cohort

  • Manchester Orthopaedics248
  • Berlin Gelenkzentrum173
  • Paris Clinique du Mouvement156
  • Bristol Joint Centre104
  • Hamburg Movement Lab67
  • Bordeaux Foot Institute52
  • London Sports Clinic31
  • Munich Ortho Campus18
  • Lyon Outcomes Centre14

Anatomic areas

5 areas · 863 procedures

  • Knee605
  • Shoulder87
  • Ankle82
  • Hip69
  • Spine20

Procedures by area

Events in the selected cohort

  • Knee605
  • Shoulder87
  • Ankle82
  • Hip69
  • Spine20

Filters update outcomes, completion, clinic benchmarking, and safety signals together.

Aggregated, pseudonymised sponsor view

Start with the sponsor view, then switch to the clinician workspace or the patient diary.

What you get

Capture EDC for proportionate investigations

Structured capture

Longitudinal ePRO and configured site forms in one programme - replace spreadsheets without buying a full Medidata-style EDC.

Automated patient flow

Scheduled follow-up, reminders and missing-data alerts so patients and sites stay on your protocol timeline.

Audit-ready exports

ALCOA+ capture, attested consent, and CSV export for proportionate pre-market and PMCF programmes.

Honest scope

Capture and review software - not a CTMS. Full eCRF query/SDV workflows sit with your CRO or partner EDC where required.

ePRO and site capture

Patient-reported outcomes and clinician baseline forms on one platform - no double entry for the data we own.

Pseudonymised by default

Patient identifiers are separated from study data so your sponsor sees a clean, defensible dataset.

End-to-end study workflow

  1. Step 1
    Step 1

    Protocol setup

    Configure PROM schedules, site capture forms, consent, and validation rules with our team.

  2. Step 2
    Step 2

    Site activation

    Set up role-based access, training materials, and a sandbox environment for each site.

  3. Step 3
    Step 3

    Patient recruitment

    Send branded patient invites, capture e-consent, and track onboarding.

  4. Step 4
    Step 4

    Data capture

    Collect ePRO and configured clinician forms with automated reminders.

  5. Step 5
    Step 5

    Review and export

    Review records, document corrections with reasons, and export CSV and regulated evidence.

  6. Step 6
    Step 6

    Analysis handoff

    Export to your CRO, biostatistician, or PMCF evaluation workflow.

Need full eCRF?For query management, SDV, and database lock, we integrate as your ePRO and engagement layer or work alongside your existing EDC partner.

Run your next study with us

Tell us about the indication, endpoints and submission target - we'll scope a study build that fits.

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