Zdrowie i gospodarka · 16/04/2014

FDA Requests Public Comment on Proposed Collection of Information for Orphan Drugs

The Food and Drug Administration (FDA) is seeking public input on a proposed collection of information related to orphan drugs, specifically the Common European Medicines Agency/Food and Drug Administration Application Form for Orphan Medicinal Product Designation (Form FDA 3671), as required by the Paperwork Reduction Act of 1995.