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FDA Puts Finishing Touches On Draft Guidance To Set Case For Quality VIP Program In Stone

 
• By Shawn M. Schmitt

The goal of the guidance is to make the Case for Quality Voluntary Improvement Program, or CfQ VIP, “more official” at the US FDA, an agency official says. CfQ VIP aims to elevate product, manufacturing and process quality at medical device firms.

A key set in stone.
• Source: Alamy

The US Food and Drug Administration is putting the finishing touches on a draft guidance document that will officially recognize a program that aims to advance quality in medical devices and their manufacturing.

“Our VIP Program – we’ve gone through several stages, we’ve gone through a pilot, and it very recently was operationalized...

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UK Healthtech Center Of Excellence Given Key MHRA Digital Regulation Role

 
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Final Curtain For LDTs? FDA Will Not Appeal District Court Decision To Vacate Final Rule

 
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FDA Drops Package Labeling Guidance For Hernia Mesh Manufacturers

 
• By Brian Bossetta

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Medtechs Wait For Dividend As UK Spending Review Prioritizes Healthcare And NHS

 
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UK Healthtech Center Of Excellence Given Key MHRA Digital Regulation Role

 
• By Ashley Yeo

Ahead of the 11 June UK spending review and its anticipated funding uplift for healthcare and life sciences, the MHRA announced an expansion of its digital expertise by creating a dedicated hub in Leeds, a renowned center of medtech excellence.