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New FDA Guidances for January 2016

Special Interest Guidances/Information Date Posted Design Considerations and Pre-market Submission Recommendations for Interoperable Medical Devices– Draft Guidance 26-Jan-2016 Postmarket Management of Cybersecurity in Medical Devices- Draft Guidance 22-Jan-2016 Guidance Agenda: Guidances CDER is Planning 22-Jan-2016 Implanted Blood Access Devices for … Continue reading

The post New FDA Guidances for January 2016 appeared first on Ask Cato Research.


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