WLF Briefing Critiques an FDA Gone Astray on Medical Device Regulation

PodiumPic1This morning, Washington Legal Foundation is hosting a Media Briefing program at 9:30, FDA Goes Astray On Device Oversight: Proposed Guidance On 510(K) Review, Adverse Events Reporting, And Recalls.

Our speakers are:

For those who cannot attend the program in person at WLF’s headquarters, below are the materials constituting press packet:

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