The SMART-TRIAL Blog

The medical device industry is rapidly developing, and we do our best to help you stay in front of the latest industry trends, best practices and regulation changes. The SMART-TRIAL Blog provides valuable insights on clinical data gathering and management as well as specific tools for data managers when designing and executing clinical studies.

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Key Pitfalls To Avoid In MedTech Clinical Data Collection Webinar with Co-Founders Jon Bergsteinsson and Pall Johannesson

7 Key Pitfalls To Avoid In MedTech Clinical Data Collection

SMART-TRIAL Releases New Add-On: Connected Devices

How to Use eConsent Efficiently in Your Medical Device Study Webinar with Pall Johannesson and Adam Steadman

How to Use eConsent Efficiently in Your Medical Device Study

PMCF data collection for lower class devices and WETs

Guide: How to Collect PMCF Data for Lower-Class Medical Devices and WETs

SMART-TRIAL Releases New eConsent Add-On

Best Practices for eConsent in Medical Device Clinical Investigations

Best Practices for eConsent in Medical Device Clinical Investigations

SMART-TRIAL Launches Version 2021.6

Adverse Event Reporting for Medical Devices

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

SMART-TRIAL Launches Version 2021.5