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Zdrowie i gospodarka · 12/06/2023

FDA Requests Public Comment on Proposed Information Collection for Allegations of Regulatory Misconduct

The Food and Drug Administration (FDA) is seeking public feedback on a proposed collection of information related to allegations of regulatory misconduct submitted to its Center for Devices and Radiological Health (CDRH), as required by the Paperwork Reduction Act of 1995.

Source: Federal Register — Food and Drug AdministrationOpen original release →