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GS1 GDSN release notes FMCG 2023/11
GDSN release note FMCG - November 2023
GS1 standards and US regulations for drug suppliers
The Drug Quality and Security Act (DQSA) went into effect on 27 November 2013 and outlines critical steps to build an electronic, interoperable system for the identification and traceability of prescription drugs as they are distributed in the US.
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Suppliers of medical devices
The medical device industry is constantly evolving and facing more and more challenges.
Unique Device Identification (UDI) is a medical device identification system used by several global regulators.
The global GS1 standards comply with national and international UDI regulations and help manufacturers comply with European regulations, US FDA regulations, and many other countries' regulations on UDI.
Unique Device Identification (UDI) is a medical device identification system used by several global regulators.
The global GS1 standards comply with national and international UDI regulations and help manufacturers comply with European regulations, US FDA regulations, and many other countries' regulations on UDI.
Other Regulations for Medical Device Suppliers
The Public Policy Database provides the latest relevant regulatory requirements, stakeholder agreements and user requests related to healthcare product identification, product catalogues and traceability at the national, regional and local levels.
It contains information collected by the global network of more than 114 GS1 member organisations (MOs), members of the GS1 Healthcare global community, government bodies and regulators involved in healthcare.
It contains information collected by the global network of more than 114 GS1 member organisations (MOs), members of the GS1 Healthcare global community, government bodies and regulators involved in healthcare.