The leading Electronic Data Capture (EDC) platform for MedTech

SMART-TRIAL is helping MedTech clinical teams to comply with regulations on clinical evidence, by simplifying the collection and management of data.

Tailor-made for MedTech, SMART-TRIAL offers a do-it-yourself Electronic Data Capture solution for clinical investigations and PMCF activities, including case-series, registries, and surveys.  

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MedTech Expertise

SMART-TRIAL has been supporting MedTech Clinical Operations since 2014, by advising and sharing expert knowledge on clinical data collection and regulatory compliance.

EDC that Mirrors Industry Needs

Offering features designed for Medical Device operations, SMART-TRIAL is building a long-term solution to fit the future of the industry and its regulatory framework.

Simplifying Compliance

With a pre-validated platform, you gain access to templates and quality files that are designed to ensure compliance with MedTech regulatory requirements.


Start your trials with HEMEX and SMART-TRIAL by digitalizing your CRF and lead the way in pioneering Electronic Data Capture in clinical studies for the future.


All-you-need eCRF for pre- or post-market clinical studies.

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Collect data directly from subjects (e.g. clinicians or patients) via email and SMS.

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Fully streamlined eCRF and ePRO for all types of clinical studies and RCTs.

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From eConsent, AE/SAE Module, Medication Module, Randomization and many additional add-ons to make the platform unique and work for you.

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GCP compliant ad hoc case-series data collection.

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GCP compliant survey-based data collection.

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Future Stars of MedTech Program

  • Unique discount schemes on all SMART-TRIAL licenses as your company grows and develops.
  • Access to the SMART-TRIAL MedTech Stars exclusive events and ready-to-use templates.
  • Receive your onboarding training with HEMEX CRO at a discounted price with support before, throughout and after your clinical trials.

This is an offer you don’t want to miss out on.

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