Intelligent Data Management for
Better Medical Devices

Illustrate the quality

of your medical device.

See it in action
Designed & developed in Denmark
with a passion for data and an eye for quality
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Made for Medical Devices

We believe that by having access to the right tools to manage data and clinical evidence, new and better devices can reach patients faster.

Flexible and Cost-Effective

Flexible license with no limits on users enable both small and large organisations to manage and collect higher quality data.

Integrate Device Data Using IoT

Integrate data from your device together with clinical data using IoT technology and the dynamic SMART-TRIAL API.

Migrate Legacy Data

Archive all studies for free. Migrate old projects or legacy data and have complete overview in SMART-TRIAL.

Single Platform for all Activities

Designed to collect and manage data throughout
the medical device life cycle

Clinical Studies

Use electronic Case Report Forms (eCRF) and electronic Patient Reported Outcomes (ePRO) to collect and manage clinical relevant data.

eCRFs » | ePRO »

Post Market Surveillance

Enroll multiple sites and collaborators to collect, document, and report outcomes on clinical efficacy, safety, and operation.

Post Market Surveillance »

Feasibility & Usability

Conduct small or early-phase studies, collect data, analyze, and prove the safety, efficacy, and usability of your medical device.

Feasibility & Usability »

Verification & Validation

With a flexible data collection toolbox, you can collect and manage data from all types of verification- and validation testing of medical devices.

Verification & Validation »
Watch the Oticon case video - 104 seconds

Driving better hearing aids faster to market

The clinical audiology department at Oticon is reducing cost and spending less time on data management

Learn how »

No more paper

Digitise the data collection and integrate data directly from your device(s). Combine electronic Case Report Forms (eCRF) with electronic Patient Reported Outcomes (ePRO) while keeping track of adverse events, concomitant medications, and device accounting.

See all features »
Save months of work

Save at least 4 hours of work for each subject, by digitising your data collection with electronic Case Report Forms (eCRF) and electronic Patient Reported Outcomes (ePRO).

Eliminate errors and missing data

Improve quality and compliance by designing better forms and customizing the data collection experience with your own company brand.

No more delays

With all your data in one place, you can re-use elements from previous projects and get started in a matter of hours.


No more meetings

Live statistics

With a live status of all sites and subjects in SMART-TRIAL you don't need to plan meetings to gain overview of the project status.

No limitations

Work with colleagues across continents in multiple languages on a platform that works on any device. There are no limits on the no. of users, sites, processes, subjects, or forms.

Reduce chaos

Evidence, whether it’s clinically related or not, is the gold of any medical device. Gain overview by archiving all projects and data in one place. Have secure access when needed, for R&D, marketing, due-diligence, or regulatory purposes.

More on security »
Digitize legacy data

With our zero risk guarantee we can migrate legacy data to a secure environment in SMART-TRIAL

Become compliant

ISO certified hosting service with state of the art medical device software quality assurance

Always available

With 24/7/365 continuous backups and 99,95% promised availability your data is always kept safe

Used by global industry leaders

Start optimising your data management today

Get Started

or take a look at the license plans