Similarities and differences between what FDA and CE certification mean

Companies expanding into the European Economic Area (EEA) need to conform to the EU regulatory requirements (CE Mark) before they can start selling their products in the territory. However many people are mislead about what the CE mark truly represents and often assume that it is equivalent to FDA approval or clearance, which is not quite accurate.

Understanding the similarities and differences between what FDA and CE certification mean will allow you to develop a more efficient and effective overall company strategy. It will also help reduce unnecessary duplication of efforts, cost and time.

To learn more about what the CE Mark is all about please go to our website at: http://mdtinternational.eu/mdt/Downloads.html