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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SMART-TRIAL Launches Version 2023.1

Medical Device Clinical Trials: Regulatory Pathways and Study Types Explained

Medical Device Clinical Trials: Regulatory Pathways and Study Types Explained

Ultimate Guide to Device Class Requirements under EU MDR

Ultimate Guide to Device Class Requirements under EU MDR

Randomization in Medical Device Clinical Trials: Everything You Need to Know

Randomization in Medical Device Clinical Trials: Everything You Need to Know

Electronic Data Capture for Medical Devices: Then vs. Now

Electronic Data Capture for Medical Devices: Then vs. Now

Tracking Serious Adverse Events for Medical Devices (to Ensure GCP Compliance)

Tracking Serious Adverse Events for Medical Devices (to Ensure GCP Compliance)

8 Tips Before Calculating Sample Size for Medical Device Studies

8 Tips Before Calculating Sample Size for Medical Device Studies

SMART-TRIAL Launches Version 2022.4

Investigator Initiated Studies Alone Are Not The Solution for PMCF Under EU MDR

Why Investigator-Initiated Studies Are Not The Solution for PMCF Under EU MDR