MADE FOR MEDICAL DEVICES

The Bridge Between Medical Devices & Clinical Data

The only Electronic Data Capture (EDC) platform designed for MedTech. A complete data collection toolbox for Post-Market Clinical Follow-Up (PMCF), Post-Market Performance Follow-Up (PMPF), Clinical Investigations and Clinical Performance Studies.

Services Overview
SMART-TRIAL PMCF database

Claiming equivalence is not enough

Ensure that your PMCF plan and clinical data will pass the scrutiny of Notified Bodies.

What clinical activity are you planning >>

Post-Market Clinical Follow-Up (PMCF)

Collect PMCF data in registries, case-series, surveys and studies.

See our complete PMCF guide here!

Pre & Post-Market Clinical Investigations

eCRF and ePRO tailor made for MedTech studies.

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Clients who trust us

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Why SMART-TRIAL?

MedTech clinical operations are Different

Made for Medical Devices

Our dedication towards MedTech is mirrored in our platform design, application, usability, licensing, support and implementation.
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Simplifying MedTech Compliance

Ready-to-use templates, modules, and features that help MedTech companies comply with industry regulations.
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Latest Updates from SMART-TRIAL & Insights on MedTech Regulatory Compliance

SMART-TRIAL

Best Practices for eConsent in Medical Device Clinical Investigations

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Updates

SMART-TRIAL Launches Version 2021.6

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Regulations

How to Ensure Efficient and Compliant Adverse Event Reporting under the EU MDR

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See All Blog Posts

Your first and only PMCF data collection tool

Learn how to collect post-market clinical data with SMART-TRIAL

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