GS1 Global Data Model
Data standard
Defines the core structure for trade items, packaging hierarchy and logistics information required for healthcare supply chains and GDSN publication.
Healthcare suppliers and medical device manufacturers operate in one of the world's most regulated industries. Accurate, standardised and compliant product information is essential for patient safety, regulatory compliance and efficient supply chain operations.
Qmica enables organisations to transform existing ERP or PIM data into GS1 and UDI-compliant product information, validate it against industry standards and publish confidently to GS1-certified data pools and healthcare partners.

Defines the core structure for trade items, packaging hierarchy and logistics information required for healthcare supply chains and GDSN publication.
Retailers often apply additional attribute requirements, validation rules and listing structures beyond the GS1 minimum. These extensions build on top of the core model.
Medical devices require regulatory identifiers such as UDI-DI, device classification and sterility status.
Hospitals depend on enriched datasets for procurement and patient safety.

Healthcare product data must meet strict regulatory and industry requirements.
Organisations often face challenges such as:

Qmica supports the product data standards commonly used within the Healthcare and Medical Devices industry.

Qmica helps healthcare organisations maintain accurate, compliant and publication-ready product information from one central platform.

Designed for manufacturers and suppliers of:
Transform, validate and publish GS1 and UDI-compliant product data with confidence.