January 2009

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We’re still feasting from our notes of the ACI Drug and Device Conference in New York last month. This post combines our thoughts with the ideas of one of the speakers at the conference. (We’re not sure if that person cares to be identified here, so we’re not naming him or her — but not

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This morning’s Washington Post, among other places, reports that there’s a movement afoot to cause the FDA to review all high-risk medical devices through pre-market approval, rather than the less rigorous pre-market notification (or “510(k)”) process.
That’s a mixed bag.
This would surely increase the time it takes to get new devices on the market,

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Back in the antediluvian days when we were in law school, the practice we learned was to include Supreme Court denials of certiori as subsequent history when citing cases in briefs. We’ve pretty much been doing it ever since.
Lately, however, we’ve seen a lot fewer “cert. denied”s in the briefs other legal stuff we’ve

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We have accidentally re-sent to subscribers to our blog a couple of old posts.

We apologize for this. We respect your time, struggle not to clutter your e-inbox, and are working to fix the technical glitch.

(We know you don’t want to hear our tale of woe, but we’re thinking of trying to upgrade to

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Once upon a time, the phrase “global coordinating counsel” was a bluff. It meant that a firm was defending hundreds of cases for a client in the United States and had recently been asked to kibbitz on one little case filed in Belgium. The guys with a marketing bent seized on this opportunity, replacing the