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Zdrowie i gospodarka · 06/05/2024

FDA Issues Final Rule on Laboratory Developed Tests and In Vitro Diagnostic Products

The FDA is amending its regulations to clarify that laboratory-developed tests (LDTs) are devices under the FD&C Act, and is phasing out its general enforcement discretion approach for LDTs to ensure the safety and effectiveness of these tests, while also considering patient access and reliance.

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