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Zdrowie i gospodarka · 03/03/2000

FDA Releases Draft Guidance on Medical Device Patient Labeling

The Food and Drug Administration (FDA) has made available a draft guidance document that outlines how to create patient labels for medical devices that are easy for patients and their caregivers to understand, with the goal of ensuring safe and effective use of these devices.

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