FDA approval
FDA approval is used for market surveillance of various product areas. Medicines, medical products and foodstuffs are particularly affected. The US Food and Drug Administration (FDA) is the publisher of the relevant guidelines.
The aim of FDA approval is to prevent adverse effects on human health through the use of the products concerned. In order to obtain FDA approval, the manufacturer himself must prove the conformity of his product.
#1 Definition Approval FDA
FDA approval defines minimum requirements for products from the medical and food sectors as well as devices directly involved in their manufacture and storage. The aim is to minimize negative influences on the human organism.
#2 Importance of FDA approval
The FDA’s requirements can have the character of law and the corresponding approval is a prerequisite for the marketability of affected products in many areas. Users within the scope of the approval therefore pay attention to FDA approval when selecting components, devices and systems.
