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Flagship Capability

Registry Management

One configurable, FHIR-native registry framework for any clinical programme, configured, not custom-built. Pre-built starter templates with built-in pathway tracking, cohort management, outcomes, and research-ready export.

More Than a Patient List

A clinical registry is your "logbook", tracking who's in your programme, where they are on their care journey, and how they're doing. Unlike EMR/EHR problem lists, registries are designed for population-level management and quality tracking.

  • Track entire patient populations, not just individuals
  • Specialty-specific data elements and workflows
  • Integrated pathway management and variance detection
  • Research-ready data extraction

Registry = Pathway + Cohort

Cohort

All patients meeting registry criteria (e.g., AFib diagnosis + anticoagulation)

+
Pathway(s)

Expected care activities, milestones, and outcomes for this population

=
Registry

Complete population management with variance detection and outcome tracking

Key Capabilities

Pre-built Starter Templates

Registry starter templates for cardiac, cancer, diabetes, chronic disease, and more, all on one configurable engine. Start from a template and tailor it to your protocols.

Cohort Management

Dynamic patient groups based on clinical criteria. Auto-enrollment when patients meet registry criteria.

Built-in Clinical Content

Validated scoring and staging where it matters, TNM (AJCC 8th ed.), Gleason, ECOG, plus automated validation that catches data issues before they reach your analytics.

Research Extraction

Export de-identified datasets for research. Pre-built formats for common research requirements.

Where schema authority lives: the project, or the platform.

A platform-level data contract

The difference between a registry that produces analytics-ready data at provincial scale and one that produces a harmonisation project later is where schema and value-list authority lives.

Project-scoped tools

Project-scoped registry tools (the REDCap pattern) centre the project as the unit of schema and value-list authority. Each project builds its own variable names, value lists, and validation rules. At provincial scale, the same clinical concept ends up with a different name and vocabulary in every project, and cross-programme analysis needs manual harmonisation downstream, every time.

Tessera

Tessera centres the platform. Concepts carry stable definitionIds and linkIds, values come from platform-managed terminologies sourced live from authoritative APIs, and validation runs at capture. The same concept maps to the same identifier across every programme and site, so cross-programme analysis is possible by default.

REDCap and similar project-scoped tools put schema and value-list authority in each project; Tessera puts it in the platform. At provincial scale, that is what keeps cross-programme analysis possible without months of harmonisation.

Pre-built Registry Starter Templates

Starter templates for common clinical programmes, all on the same configurable engine. Start from one and tailor it to your protocols, or scaffold a new programme.

❤️

Atrial Fibrillation

Anticoagulation management, rhythm control, CHADS-VASc tracking

🫀

Cardiac Surgery

Pre-op optimisation, ERAS protocol, post-op recovery tracking

💓

Heart Failure

GDMT optimisation, fluid management, readmission prevention

🩺

Cath Lab

PCI outcomes, stent tracking, ACS pathways

🎗️

GU Cancer

Staging, treatment protocols, surveillance pathways

🎀

Breast Cancer

Screening, treatment coordination, survivorship care

🩸

Diabetes (Pediatric)

A1c tracking, insulin management, transition to adult care

💊

Chronic Pain

Multi-modal treatment, opioid stewardship, functional outcomes

🫁

Organ Donation

Donor management, organ allocation tracking

🚑

Trauma

Injury severity, resuscitation protocols, outcomes tracking

🧠

Stroke

Door-to-needle time, rehab milestones, secondary prevention

📋

PROMs/PREMs

Patient-reported outcomes and experience collection

Complete Registry Lifecycle

Patient Enrollment

  • Manual enrollment by care team
  • Auto-enrollment via FHIR triggers
  • Bulk import from EMR/EHR
  • Waitlist management

Data Collection

  • FHIR-synced clinical data
  • Custom data capture forms
  • PROM/PREM questionnaires
  • Document upload

Pathway Integration

  • Pathway assignment per registry
  • Milestone tracking
  • Variance detection
  • Goal monitoring

Analytics & Reporting

  • Registry dashboards
  • Quality indicators
  • Outcome reports
  • Research data export

FHIR Resources

Group→ Registry cohort membership
ServiceRequest→ Registry enrollment
Observation→ Clinical data points
QuestionnaireResponse→ PROMs/PREMs

Data That Flows

Registry data syncs with your EMR/EHR through FHIR R4. Clinical observations, questionnaire responses, and pathway status all flow automatically.

  • Dynamic cohort filtering based on clinical criteria
  • Bi-directional sync with EMR/EHR data
  • Research-ready export with de-identification

Ready to Launch Your Registry?

Book a demo to see how registry management can help you track populations and improve outcomes.