Federal Register #FDA-2025-N-2220

FDA Seeks Public Comment on Information Collection for Medical Device and Radiation-Emitting Product Communications

The Food and Drug Administration (FDA), under the Department of Health and Human Services, is seeking public comment on its proposed information collection for testing communications about medical devices and radiation-emitting products. - Government Buyer: - Food and Drug Administration (FDA), Department of Health and Human Services - Purpose: - Collect feedback to improve communication strategies and materials related to medical devices and radiation-emitting products - Methods: - Research methods include in-depth interviews, focus groups, intercept interviews, self-administered surveys, gatekeeper reviews, and omnibus telephone surveys - Participants: - Target audiences are consumers, caregivers, and healthcare professionals - Products/Services Requested: - No physical products or services are being procured - The request is for public input on information collection and communication effectiveness - OEMs and Vendors: - No specific Original Equipment Manufacturers (OEMs) or vendors are named in this notice - Notable Requirements: - Focus is on evaluating and improving FDA communications, not on purchasing goods or services

Description

The Food and Drug Administration (FDA) is announcing the submission of a proposed collection of information to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995. The collection involves testing communications on medical devices and radiation-emitting products using various research methods such as interviews, focus groups, and surveys. The information collected will be used to develop, test, and evaluate communication strategies and messages targeted at consumers, caregivers, and healthcare professionals. Comments on the collection are requested by June 10, 2026.

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