White Paper

Medical Device Labeling - Regulations In The U.S., EU, And China

Source: Mettler-Toledo Product Inspection

By Oliver Wyrsch

Medical Device Labeling - Regulations in the U.S., EU, and China

This white paper explores the labelling requirements for medical devices in the United States, the European Union, and China. Each territory has its own particular set of regulations governing the labeling of medical devices, and while there are a certain amount of commonalities in each of the regulations, there are differences which necessitate care from global manufacturers when distributing products.

Mettler-Toledo Product Inspection