Richard Burr: “The decision underscores how military commanders are scrambling to meet President Obama's order.”

The faster, more predictable, and more accountable the programs are, the more patients stand to benefit from lifesaving, innovative drugs and devices.

What does it mean for a small company when FDA misses these goals, and what does it mean to patients?

When is somebody going to share with the American people the destination we are trying to get to and how we are going to get to that destination?

Why did FDA agree, and why did the industry agree to longer review times of 128 days on 510(k)'s and provide the agency with so much more money?