Regulatory workshop on medical devices: COMPLIANCE CHECK OF MEDICAL DEVICES PRIOR TO MAKING THEM AVAILABLE IN THE MARKET

Third term: 26th March 2020 – CANCELLED (COVID-19)
raPHARM premises, 30 Miklošičeva Street, Ljubljana (Slovenian language)

Fourth term: 9th April 2020
raPHARM premises, 30 Miklošičeva Street, Ljubljana (Slovenian language)

 

Regulatory workshop on medical devices
COMPLIANCE CHECK OF MEDICAL DEVICES PRIOR TO MAKING THEM AVAILABLE IN THE MARKET

The workshop is intended for all economic operators (distributors, importers, authorized representatives, and manufacturers) involved in the supply chain of medical devices and who need practical skills for checking the compliance of requirements they need to check for devices before making them available in the market.

The practical skills and the relevant templates will help you check whether the products in your portfolio are compliant with the Regulation (EU) 2017/745, focusing on:

  • their CE marking,
  • the content of the EU Declaration of conformity of the device,
  • the information provided with the device,
  • information supplied by the importer and
  • assigning a unique device identifier – UDI.

Click HERE for more information on the workshop.

Click HERE to apply for the workshop.