Knowledge center Healthcare

• Registration GS1 Belgium & Luxembourg
• Registration My Product Manager
• Start entering data
• Start receiving data
• Sharing product information in the healthcare sector

Medical devices

• Step-by-step plan for a Unique Device Identifier (UDI)
• FAQ UDI-DI & Basic UDI-DI

Medicines

• Identification of medicines
• Identifying medicines uniquely - Steps plan
• Identifying medicines uniquely - Manual
• Medicines suppliers - FAQ

Europe

• EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) 
• Falsified Medicines Directive & GS1 standards for medicine suppliers

US

• US legislation Food and Drug Administration (FDA) 
• GS1 standards and US regulations for drug suppliers 

UK

• United Kingdom regulations National Health Services (NHS)
• UK reglementation National Health Services (NHS) (Brexit)

Other

• Other Regulations for Medical Device Suppliers 

• Codes for Intrastat
• Codes for packaging (RTI)
• Codes international quality marks
• Codes for packaging types
• Codelist taxes
• Codelists My Product Manager

• GS1 ECHO datamodel & validation rules
• Useful documentation healthcare
• Applications & tools 

• E-learning: learningplan for the healthcare sector in Belgilux