Workshop on EU Medical Device and In Vitro Diagnostic Regulations
2023-03-16
Online, 15:30-18:30 (UTC+8) / 08:30-11:30 (UTC+1)
The deadline for registration on the website has passed - please feel free to contact qi-china@giz.de directly if you would like to participate.
We cordially invite you to the virtual workshop EU Medical Device and In Vitro Diagnostic Regulations. The event is organised by Shenzhen Customs and the Global Project Quality Infrastructure.
Mr Ortwin Schulte, Division Director for Medical Products Safety at the German Federal Ministry for Health, will inform on the latest regulatory developments in this area and be available for questions.
The workshop will be held in English with simultaneous interpretation into Chinese during the presentation and consecutive interpretation during the Q&A session.
Date: Thursday, 16 March from 15:30-18:30 (UTC+8) / 08:30-11:30 (UTC+1)
Registration: The event is free of charge. Please kindly use the registration form below to sign-up for the event until 14 March.