GS1 Workshop EU-UDI – in collaboration with beMedTech – 24/10/2017.

Recently the EU has issued new mandatory regulations for medical devices and medical devices for in-vitro diagnostics. these include a major modification regarding the application of a Unique Device Identifier (UDI) on (the packaging of) medical devices. In order to assist manufacturers in preparing the UDI, GS1 Belgium & Luxembourg sets up a workshop in collaboration with beMedTech.

Program:

  • 09h00: Welcome with coffee
  • 09h30: Introduction (beMedTech & GS1)
  • 09h40: New regulations of the EU UDI system for medical devices
    GĂ©raldine Lissalde-Bonnet, GS1 Global Office.
  • 10h10: GS1 standards as a tool for compliance with the EU UDI system.
    Ann Luyckx, GS1 Belgium & Luxembourg
  • 10h45: break
  • 11h00: EU MD Regulations; what does it mean for the hospitals?
    Hospital Pharmacist (tbc)
  • 11h45: UDI in practice; experience from a manufacturer.
    Manufacturer (tbc)
  • 12h30: Closure (beMedTech / GS1)
  • 12h40: Lunch.

Location: Business Faculty; Sint-Lendriksborre 6 Font Saint Landry – 1120 Brussels (Neder-Over-Heembeek)

To register click here.