For Clinical Researchers

Stop losing data to survey fatigue. Start capturing it in real-time.

REDCap and legacy ePRO tools suffer from 27-40% missing data rates. Forma Health replaces episodic surveys with continuous, AI-powered patient data collection — structured, normalized, and analysis-ready from day one.

See Your Study Configured

Custom demo · Your condition · Set up in under 1 hour

By the Numbers

<8 weeks

Average deployment time vs. 3-6 months for enterprise ePRO

80%+

Patient completion rates for longitudinal studies

Hourly

Data resolution — continuous event logging vs. weekly survey windows

Why Forma for Research

Better data starts with better collection

Faster path to ‘why’

Surveys exhaust respondents before capturing enough data to answer ‘why.’ Forma Health captures 100× more data points — so when unexpected results appear, you have the granularity to investigate causes, not just correlations.

Insights from the start

With Forma, patient-entered data is normalized, structured, and mapped to international vocabularies within seconds. Start developing insights while the trial is in progress — don’t wait for end-of-study data processing.

Research-grade data quality

CONSORT-PRO and SPIRIT-PRO compliant by default. Data maps to FHIR, SNOMED, and common data models. Built for regulatory submissions, interoperability, and future meta-analysis.

Who We Serve

Purpose-built for every stage of clinical research

Foundations & Advocacy Groups

"Build the dataset pharma will license."

  • Custom app for community symptom tracking
  • High-fidelity longitudinal data ready for regulatory submission
  • Foundation controls data; pharma licenses separately
  • Setup and validation done in only days

Academic PIs & KOLs

"Pioneer insights and improve outcomes."

  • Track daily fluctuations and specific patient outcomes
  • Capture context and environmental input
  • Fill in the gaps for validated surveys
  • Automated reminders that improve adherence

Pharma

"Understand factors that impact individual patient responses."

  • Regulatory-grade data (21 CFR Part 11, PMR-ready)
  • Eliminate survey fatigue and increase patient participation
  • Proactive adverse event detection
  • Seamlessly connect to existing data tools

Why Researchers Choose Forma

Purpose-built to replace tools that weren't designed for longitudinal patient data

vs

REDCap

Free but costly in data quality

  • Automated reminders (vs. manual follow-up)
  • Mobile-first patient experience
  • Built-in correlation analytics
  • 27-40% less missing data

vs

Enterprise ePRO

Medidata, Signant, Clario — overbuilt, overpriced

  • Deploy in <8 weeks (vs. 3-6 months)
  • Purpose-built for Phase 4 and academic
  • Built-in analytics and visit-prep
  • Fraction of the cost

vs

Hospital PRO Platforms

PatientIQ, CODE — hospital-focused, not research-grade

  • Research-grade data + clinical utility
  • Cross-segment applicability
  • Patient value = engagement = better data
  • FHIR-native and interoperable

Use Cases

Clinical Trials (ePRO+)
Natural History Studies
Long-haul Studies
Post-Market Surveillance (Phase 4)
Real-World Evidence (RWE)

See how Forma configures for your study

Custom demo with your condition, your endpoints, your data needs — set up in under an hour.