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Zdrowie i gospodarka · 18/07/2022

FDA Releases Draft Guidance on Residual Solvents in Veterinary Medicinal Products

The US Food and Drug Administration (FDA) has made available a draft guidance document (GFI #100) outlining acceptable levels of residual solvents in new veterinary medicines, developed in collaboration with the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH)

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