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Info on Orphan Drug Form Sent to OMB

04/30/2008

Federal Register Notice: FDA’s proposed collection of information, “Orphan Drugs; Common European Medicines Agency/Food and Drug Administration Application Form for Orphan Medicinal Product Designation (Form FDA 3671)” has been submitted to the Office of Management and Budget for review and clearance under the Paperwork Reduction Act of 1995. To view this notice, click here.

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