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 info@verlabinstitute.com 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.

Digital Innovation Hubs

LabHub

Technology

  • Data analytics
  • Artificial Intelligence
  • Others

Technique

  • Webinar

Channel

  • Online

Technology Absortion Cycle

  • Operation
  • Updates on configuration and operation

Target Group

  • Other

Instruction Level

  • Foundation
  • Intermediate
  • Advanced
  • Highly Specialized

Sector

  • Research & Development

Education Level

  • Bachelor
  • Master
  • PhD

Capacity

  • 5 to 10

Details

Website

dmbiubih@gmail.com

Date: Upon request

Durations: 1h to 4h, 1-3 days

Price: 250€ per person


Project

Other

Countries where training is provided

Cities where training is provided

Languages this training can be provided

English

Imagen


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