Get started Registration GS1 Belgium & LuxembourgRegistration My Product ManagerStart entering dataStart receiving dataSharing product information in the healthcare sectorMedical devicesStep-by-step plan for a Unique Device Identifier (UDI)FAQ UDI-DI & Basic UDI-DIMedicinesIdentification of medicinesIdentifying medicines uniquely - Steps planIdentifying medicines uniquely - ManualMedicines suppliers - FAQ Regulations EuropeEU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) Falsified Medicines Directive & GS1 standards for medicine suppliersQ&As on practical aspects related to the implementation of Regulation (EU) 2024/1860 EUDAMEDUSUS legislation Food and Drug Administration (FDA) GS1 standards and US regulations for drug suppliers UKUnited Kingdom regulations National Health Services (NHS)UK reglementation National Health Services (NHS) (Brexit)OtherOther Regulations for Medical Device Suppliers Codelists Codes for IntrastatCodes for packaging (RTI)Codes international quality marksCodes for packaging typesCodelist taxesCodelists My Product Manager Data model, manuals, legal texts, applications and tools GS1 ECHO datamodel & validation rulesUseful documentation healthcareApplications & tools Training & webinars E-learning: learningplan for the healthcare sector in Belgilux Questions? Contact the helpdesk +32 2 896 52 14 healthcare@gs1belu.org
