Certificación CE y certificación 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.

De Amerikaanse Food and Drug Administration (Food and Drug Administration) wordt afgekort als FDA, een van de door de Amerikaanse regering opgerichte uitvoerende agentschappen in het Department of Health and Human Services (DHHS) en het Department of Public Health (PHS) . Als wetenschappelijk managementbureau is het de verantwoordelijkheid van de FDA om de veiligheid te garanderen van voedsel, cosmetica, medicijnen, biologische agentia, medische apparatuur en radioactieve producten die in de Verenigde Staten worden geproduceerd of geïmporteerd. Het is een van de eerste federale instanties met als belangrijkste functie het beschermen van consumenten.