MADE FOR MEDICAL DEVICES

Get closer to your PMCF data

The leading Electronic Data Capture (EDC) platform for MedTech. A complete data collection toolbox for Post-Market Clinical Follow-Up and Clinical Investigations.

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

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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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SMART-TRIAL

SMART-TRIAL launches ISO14155:2020 Compliant AE Reporting Module for Medical Device Studies

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SMART-TRIAL

How to Conduct a Successful Post-Market Clinical Follow-Up (PMCF) Survey

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Regulations

Overview of the new Guidance documents from MDCG on Clinical Investigations and Evaluations

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Latest updates from
SMART-TRIAL & Insights on MedTech Regulatory Compliance

Your first and only PMCF data collection tool

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

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