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.

Streamlined eCRF & ePRO for PMCF Studies and Clinical Investigations

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.

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

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

Popular Add-ons for Suite

eConsent

Electronic Informed Consent process

AE

Adverse Event Reporting

Translate

Translations Module

Try It For Free!

Streamlined eCRF & ePRO for PMCF Studies and Clinical Investigations

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

eCRFValidate device usability, design & general application in clinical practice.

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

ePROBuild a dataset of patient outcomes

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

Popular Add-ons for Suite

eConsent

Electronic Informed Consent process

AE

Adverse Event Reporting

Translate

Translations Module

Try It For Free!

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

ePRO
Build a dataset of patient outcomes