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HHS Guidance Submissions

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Title OpDiv/StaffDiv Sort descending Guidance Status Issue Date
Electrocardiograph (ECG) Surface Electrode Tester  Food and Drug Administration (FDA) Final
Electronic Drug Product Reporting for Human Drug Compounding Outsourcing Facilities Under Section 503B of the Federal Food, Drug, and Cosmetic Act.”  Food and Drug Administration (FDA) Final
Elemental Impurities in Drug Products Guidance for Industry  Food and Drug Administration (FDA) Final
Emission Delay - Remote Interlock Connector (Laser Notice 21)  Food and Drug Administration (FDA) Final
Emission Indicator - Visibility (Laser Notice 10)  Food and Drug Administration (FDA) Final
Emission Indicators - Brightness (Laser Notice 6)  Food and Drug Administration (FDA) Final
Emission Indicators on Energy Source (Laser Notice 3)  Food and Drug Administration (FDA) Final
Emitted Laser Beam as Emission Indicator for Class II and Class IIIa Laser Products (Laser Notice 49)  Food and Drug Administration (FDA) Final
End-of-Phase 2A Meetings  Food and Drug Administration (FDA) Final
Endotoxin Testing Recommendations for Single-Use Intraocular Ophthalmic Devices  Food and Drug Administration (FDA) Final
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