Business · 15/11/2019Updated: 10/17/2026 · 1 min read
FDA Announces Proposed Collection of Information for Medical Devices Under Paperwork Reduction Act
Summary
The Food and Drug Administration (FDA) is announcing a proposed collection of information for review and clearance under the Paperwork Reduction Act of 1995, as part of the Q-Submission Program for Medical Devices, and is seeking public comment.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →