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 for clinical investigations and PMCF activities, including case-series, registries and surveys.
SMART-TRIAL has been supporting MedTech Clinical Operations since 2014, by advising and sharing expert knowledge on clinical data collection and regulatory compliance.
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.
With a pre-validated platform, you gain access to templates and quality files that are designed to ensure compliance with MedTech regulatory requirements.
Collect data directly from subjects (e.g. clinicians or patients) via email and SMS.
learn moreFrom 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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