Certification CE et certification FDA

CE certification, which is limited to the basic safety requirements of products that do not endanger the safety of humans, animals and goods, rather than the general quality requirements, the harmonized directive only stipulates the main requirements, which are standard tasks. Therefore, the accurate meaning is: the CE mark is a safety mark instead of a quality mark. It is the "main requirement" that forms the core of the European Directive.

The "CE" mark is a safety certification mark and is regarded as a passport for manufacturers to open and enter the European market. CE stands for European Unification (CONFORMITE EUROPEENNE).

The "CE" mark in the EU market is a mandatory certification mark. Whether it is a product produced by an enterprise within the EU or a product produced by another country, if it is to be circulated freely in the EU market, it must be affixed with the "CE" mark to indicate that the product Comply with the basic requirements of the EU "Technical Coordination and Standardization New Method" directive. This is a mandatory requirement imposed on products by EU law.

La Food and Drug Administration des États-Unis (Food and Drug Administration) est abrégée en FDA, qui est l'une des agences exécutives établies par le gouvernement américain au sein du Department of Health and Human Services (DHHS) et du Department of Public Health (PHS) . En tant qu'agence de gestion scientifique, la FDA a pour responsabilité d'assurer la sécurité des aliments, des cosmétiques, des médicaments, des agents biologiques, des équipements médicaux et des produits radioactifs produits ou importés aux États-Unis. C'est l'une des premières agences fédérales dont la fonction principale est de protéger les consommateurs.