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.

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

Choose the experience built for your role.

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.

CNS / neurology

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.

Not sure where to start?

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.