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Zdrowie i gospodarka · 08/03/1999

FDA Releases Guidance Document for Biological In Vitro Diagnostic Products

The FDA has released a guidance document to provide industry with clear guidelines on the content and format of chemistry, manufacturing, and controls information and establishment description for biological in vitro diagnostic products, aiming to reduce unnecessary burdens while maintaining public health protection.

Source: Federal Register — Food and Drug AdministrationOpen original release →