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Zdrowie i gospodarka · 26/07/1999

FDA Releases Draft Guidance on Monoclonal Antibody Products Under Orphan Drug Regulations

The Food and Drug Administration (FDA) has released a draft document outlining its criteria for determining the sameness of monoclonal antibody products under the Orphan Drug Act and implementing regulations, aimed at providing clarity for sponsors and manufacturers.

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