Medical device post-market surveillance: Inspection of medical devices for regulatory purposes

Initiative Description

Training on medical device post-market surveillance focusing on inspection of medical device performance according to ISO 17020. The training is provided in partnership with Verlab Research Institute through the module - Verlab Academy! All information available via [email protected] and www.verlabinstitute.com.

Training Objectives

Train and provide novel skills to clinical engineers, healthcare professionals and researchers in post-market surveillance of medical devices (inspection of performance)helping in digital transformation of clinical engineering field.

Training Contents

Medical technology performance and safety requirements - understanding; Metrology in medical device post-market surveillance; Legal metrology for medical device performance inspection according to ISO 17020.