Zdrowie i gospodarka · 12/03/2003
FDA Requests Public Comment on Proposed Collection of Information for Investigational Device Exemptions Reports and Records
The Food and Drug Administration (FDA) is seeking public input on its proposed collection of information related to investigational device exemptions (IDE) reports and records, as required by the Paperwork Reduction Act of 1995.
Source: Federal Register — Food and Drug AdministrationOpen original release →