CE-certifiering och FDA-certifiering

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.

USA: s livsmedels- och drogadministration (Food and Drug Administration) förkortas till FDA, som är en av de verkställande organ som inrättats av den amerikanska regeringen i Department of Health and Human Services (DHHS) och Department of Public Health (PHS) . Som en vetenskaplig förvaltningsbyrå är FDA: s ansvar att säkerställa säkerheten för livsmedel, kosmetika, läkemedel, biologiska medel, medicinsk utrustning och radioaktiva produkter som produceras eller importeras i USA. Det är en av de tidigaste myndigheterna vars huvudfunktion är att skydda konsumenterna.