Zdrowie i gospodarka · 12/12/2007

FDA Submits Proposed Collection of Information for Certification to Accompany Drug, Biological Product, and Device Applications

The Food and Drug Administration (FDA) has submitted a proposed collection of information to the Office of Management and Budget (OMB) for emergency review under the Paperwork Reduction Act of 1995, related to the certification required for human drug, biological product, and device applications or submissions.