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FDA Trends & Developments for the Medical Device Industry: 2016

A Guide to Recent FDA Initiatives & Advice for Industry Leaders

The regulatory environment is in a state of transition. New technologies, growing cost pressures and quickly-shifting consumer expectations are just a few of the factors driving changes in medical device manufacturing and regulatory compliance both domestic and abroad.

We've gathered the top FDA trends and developments for 2016 into this go-to guide along with advice from industry experts and on how these initiatives will affect medical device companies large and small.

What you'll find inside:

• Actionable summaries of the top ten FDA initiatives for medical device companies in 2016
• Key takeaways from recent FDA Guidance documents
• Advice from industry experts and Former FDA personnel