Business · 19/03/2012Updated: 10/17/2026 · 1 min read
FDA Announces Guidance for Medical Device ISO 13485:2003 Voluntary Audit Report Submission Pilot Program
Summary
The FDA is releasing a guidance document outlining the implementation of the Food and Drug Administration Amendments Act of 2007, which amends the Federal Food, Drug, and Cosmetic Act, and the Pilot Program will begin on June 5, 2012.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →