Certified medical device
GDPR-compliant

The app platform for your clinical trial

Whether for data collection, symptom tracking, or control arm intervention - a certified solution that adapts to your study design.

ePRO

Symptoms

Wearables

Control arm

The facts at a glance

Get started

No in-house development

Ready-to-use infrastructure – pilot launch typically within a few weeks.

Indications

< 100 ICDs

From cancer to rheumatism or IBD - new conditions are added constantly and integrated within a few weeks

Savings

Time & Budget

No need to develop or maintain your own solution – saving both budget and preparation time.

Quality

GCP-ready

Structured, auditable data collection meeting the requirements of clinical trials.

Data Privacy

GDPR-compliant

Encrypted storage, servers in Frankfurt (EU-West-1), data processing agreements available upon request.

Regulatory Approval

Medical Device

Certified and ready for use in studies across various fields and indications

Study Design

Three ways Fimo Health fits into your study

Data collection

Structured collection of patient-reported outcomes, symptoms, and wearable data. Configurable to your study protocol, with reminders and live dashboards for your study team.

Intervention

The certified app, for example as a comparator intervention in the control arm – including evidence-based modules (SMART goals, ACT/CBT). Ready to use with no internal development required, with a documented scope of services.

Consortium partner

Planning a funded research project? We can work together to develop dedicated features or custom app versions – MDR-compliant, backed by experience from BMBF, state, and EU-funded collaborative projects.

Holistically support subjects as part of your research project?

EDC Integration

Seamless data flow from the app directly into your EDC system – GDPR-compliant, automated, and GCP-ready.

Configurable

From questionnaires to collection intervals: flexibly adapt the app to your scientific study design.

Wearable & Environmental Data

Integrates common wearables and supplements data collection with context data such as environmental or weather information – for a more complete picture than self-reporting alone.

Learning Journeys

Structured, evidence-based learning content guides participants through the study – from psychoeducation to concrete coping strategies.

Reminders

Smart re-engagement ensures continuous data entry and high adherence throughout the entire study duration.

Dashboards

Keep an eye on study progress, data quality, and patient compliance at all times.

Frequently Asked Questions

Can the app be customized?

The basic version is ready for immediate use. We would be happy to discuss your requirements for further customizations.

How quickly can a study be launched?

Following the initial consultation, configuration typically takes a few weeks until the pilot phase—depending on the scope of the study.

Does Fimo Health provide support with grant applications?

Yes, for consortium projects, we bring experience from BMBF, state, and EU-funded collaborative projects, including sub-project descriptions and budget calculations.

Can the data be transferred to our existing EDC system?

Yes, data is transferred in a structured and automated manner into your EDC system via a GDPR-compliant connection.

How are study participants motivated to use the app?

Automated reminders and an accessible, user-friendly app experience ensure consistent adherence throughout the duration of the study.

How is data protection ensured?

Development and operations are GDPR-compliant, with processing carried out in accordance with the study protocol and data processing agreement.

Interest sparked?

Find out more or contact us directly.