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  • Solutions

One platform. Two tailored experiences.

ProCTTH meets each stakeholder where they work. Sites get an engagement-first eSource; sponsors and CROs get a blinded eCRF with real-time operational visibility — on the same unified data model.
For Sites
For Sponsors / CROs
  • Our vision

ProCTTH is changing the future of the clinical trial ecosystem by integrating end-to-end clinical trial flow through technology — with, clinical sites at the center.

Subject retention
0 %
Less monitoring time
0 %
To database lock
0 days
PII exposed
0
  • Pick your path

Choose the experience built for your role

  • For Clinical Sites

eSource that engages your subjects

Capture source data once, schedule visits, chat with subjects, and reward retention — all while subject identity stays at the site.

  • Coordinator command center
  • ProCoins retention engine
  • No-code study setup
  • IoT & wearables capture
Explore for Sites
  • For Sponsors & CROs

Blinded eCRF with real-time visibility

Clean, audit-ready data the moment it’s captured. Run hybrid and decentralized trials without ever exposing PII.
  • Real-time eCRF + SDV
  • KRI dashboards
  • 21 CFR Part 11 & GCP
  • Multi-region data residency
Explore for Sponsors / CROs
  • Shared foundation

What every stakeholder gets.

Compliance baked in

21 CFR Part 11, GCP, HIPAA, and GDPR on day one — with a validation pack ready to ship.

One unified data model

Subjects, visits, devices, and audit events live in a single schema — no per-study silos or exports.

Hybrid & DCT ready

E-consent, home visits, IoT capture, and mobile engagement ship out of the box.

Global by design

Deploy to EU, US, India, Japan, or Canada with regional data residency controls.

Role-based access

Super Admin, Admin, Study Admin, Member, Investigator, CRA, CRC, and Subject — all scoped.

AI where it earns its place

Protocol-to-form generation, eligibility matching, and drop-off prediction — reviewer-in-the-loop.

  • Therapeutic coverage

Proven across therapeutic areas.

  • Rare disease
Global recruitment, multi-language consent, and patient-reported outcomes for small cohorts.
  • Oncology
Visit-heavy schedules, complex labs, and real-time safety signaling.
  • Cardio-metabolic
Wearables + IoT vitals streamed into visit forms with anomaly detection.
  • Cardio-metabolic
Digital cognitive assessments, caregiver ePRO, and adherence monitoring.
  • Vaccines
Large-cohort e-consent, diary cards, and reactogenicity reporting.
  • Medical device
IoT device pairing, firmware logs, and usability capture at the source.

Let's map ProCTTH to your workflow.

A 30-minute walkthrough with our clinical operations team. We’ll show you exactly how sites, sponsors, and CROs collaborate on a single platform.
Book a walkthrough
See pricing

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