Streamlined eCRF & ePRO for PMCF Studies and Clinical Investigations

Seamlessly integrate eCRF and ePRO to collect clinical data from both healthcare staff and patients.

Integrate eCRF & ePRO

  • Interlace ePRO events with scheduled Study visits
  • Automatic send out of patient questionnaires
  • Create new entries directly from the eCRF
  • Overview of all data collection activities
  • Data safely stored in one central location

eCRF
Validate device usability, design & general application in clinical practice.

Clinical data entry from clinicians and healthcare staff from eCRF

  • Create Forms to gather information about general usability, design, and clinical application (depending on device).
  • Likert scale for usability and design related questions
  • Make amendments on the go
  • Flexible and customisable roles and permissions

ePRO
Build a dataset of patient outcomes

Combine clinical information with patient-reported outcomes, to build a solid registry around the usage and efficacy of your device

  • Improve the quality of data for regulatory affairs
  • Improve customer experience with your device
  • Improve overview of the device performance in the market
  • Follow-ups with Automation & Reminders
  • Public sign up or normal subject events

Validation & Reference Rules

Set up advanced validation rules on individual questions.Trigger SMART-TRIAL to automatically show a warning message, create a query, or block the data input.

Popular Add-ons for Suite

eConsent

Electronic Informed Consent process

Enhance the informed consent process using electronic signatures.

Learn more

AE

Adverse Event Reporting

Ready-to-use MDR and ISO 14155:2020 AE teamplate with automatic rules and notifications.

Learn more

Translate

Translations Module

Enable your users and subjects to deliver data in their own language.

Learn more

Try It For Free!

Book your customized demo here

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