Get started 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 Regulations 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 Data model, manuals, legal texts, applications and tools GS1 ECHO datamodel & validation rules Useful documentation healthcare Applications & tools Training & webinars E-learning: learningplan for the healthcare sector in Belgilux Questions? Contact the helpdesk +32 2 896 52 14 healthcare@gs1belu.org