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Frequently asked questions:
eCRF templates for clinical trials
What is EDC (Electronic Data Capture) and how does Tiro.health's approach differ?
EDC refers to systems that collect clinical trial data electronically instead of on paper. Traditional EDC platforms require sites to log into separate systems and duplicate data entry from patient records into study forms.
Tiro.health's EDC approach is different because our eCRF templates integrate directly into hospital EHR systems. Investigators capture trial data during normal patient care within their existing workflow, eliminating duplicate data entry and improving compliance.
Tiro.health's EDC approach is different because our eCRF templates integrate directly into hospital EHR systems. Investigators capture trial data during normal patient care within their existing workflow, eliminating duplicate data entry and improving compliance.
How do eCRFs work within existing hospital systems?
Electronic Case Report Forms (eCRFs) are the digital forms used to collect patient data during clinical trials. Instead of requiring separate logins and systems, our eCRFs embed directly into hospital EHR interfaces using FHIR integration.
When a doctor sees a trial patient, the study form appears within their normal documentation workflow. Data captured is automatically structured, coded with medical terminology (SNOMED CT), and flows to your study database in real time.
When a doctor sees a trial patient, the study form appears within their normal documentation workflow. Data captured is automatically structured, coded with medical terminology (SNOMED CT), and flows to your study database in real time.
What's the difference between CRF and eCRF?
A Case Report Form (CRF) is the traditional paper form used to collect trial data. An eCRF is the electronic version of the same form.
Our eCRFs go beyond simple digitization. They include built-in data validation, automatic medical coding, and integrate with hospital terminology systems to ensure data quality and consistency across all trial sites.
Our eCRFs go beyond simple digitization. They include built-in data validation, automatic medical coding, and integrate with hospital terminology systems to ensure data quality and consistency across all trial sites.
Is the medical form builder GDPR compliant for European healthcare?
Our healthcare form platform is fully GDPR compliant with ISO 27001 certification, European data residency, and enterprise-grade security.
All medical data processing meets European healthcare data protection standards and EHDS (European Health Data Space) requirements.
All medical data processing meets European healthcare data protection standards and EHDS (European Health Data Space) requirements.
What is FHIR and why does it matter for clinical trials?
Fast Healthcare Interoperability Resources (FHIR) is the modern standard for healthcare data exchange. It allows our eCRF platform to integrate with any hospital's EHR system regardless of vendor.
For clinical trials, this means you can deploy consistent data collection across sites using different hospital IT systems without custom integrations or lengthy IT negotiations.
For clinical trials, this means you can deploy consistent data collection across sites using different hospital IT systems without custom integrations or lengthy IT negotiations.
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Use our structured data platform for seamless eCRF deployment across diverse hospital networks and EHR systems