FDA Draft Guidance Would Set In Stone Case For Quality Voluntary Improvement Program

The draft document from the US agency looks to officially recognize a program aimed at advancing quality in medical devices and their manufacturing.

Female with name tag, hello my name is - Image

The US Food and Drug Administration on 5 May released a draft guidance document to officially recognize a program that aims to advance quality in medical devices and their manufacturing.

The 18-page draft, “Fostering Medical Device Improvement: FDA Activities and Engagement with the Voluntary Improvement Program,” carries a date...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Medtech Insight for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Regulation

More from Policy & Regulation