The SMART-TRIAL Blog

Category:

||||||||||

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

PMCF Survey||

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

||||

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

Calculate sample size|

How to calculate Sample Size for Medical Device Studies

|||||

How technology can support MedTech clinical trial continuity & data integrity

SMART-TRIAL 2020.1 release||

SMART-TRIAL 2020.1 is now available

Investigator Initiated Studies - Generate MDR compliant clinical data

Clinical studies

Investigator-Initiated Studies - A way to generate MDR compliant clinical data

Clinical studies

7 tips to improve the collection of clinical data for your Medical Device

The Current Status of MDR Clinical Guidance

1 / 7