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.

For further information, see public-policy database.


EU Medical Device Regulation (MDR) & in-vitro diagnostics (IVDR)


UK regulation National Health Services (NHS)


US regulation Food and Drug Administration (FDA)