All I can say, as I mentioned earlier, is that in 2004 when we looked at medical devices, we did look at the activities for licensing, and we found that the department was carrying out all of the procedures in accordance with their own policies. Now, should they decide to have an independent committee, that would certainly supplement, perhaps, the rigour with which this is done. But we did not see any indication of difficulties in their following through on their own process. The concern at the time seemed to be more the time that it took something to get to market actually, and the delays in that process.
On April 10th, 2008. See this statement in context.