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Zdrowie i gospodarka · 07/05/2008

FDA Announces Proposed Collection of Information for Device Registration Under Paperwork Reduction Act

The Food and Drug Administration (FDA) has submitted a proposed collection of information to the Office of Management and Budget (OMB) for emergency processing, requiring device establishments to submit registration and listing information electronically by 2024, unless granted a waiver by the Secretary of Health and Human Services.

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