I can honestly say that our mandate is to regulate prices, but we currently have a discussion paper out there for all our stakeholders, which goes to re-benching, re-looking at the price of a medication once it's been on the market for a number of years.
As you alluded, Mr. Brown, after the drug's been out there for several years, obviously, some of the things that have not been picked up in the clinical trials come to the surface: either the drug becomes less effective or it becomes more effective for perhaps another indication. Would that be an occasion when the pharmaceutical manufacturer might ask for an increase in his price? Conversely, we might determine that the drug is not as effective as projected and lower the price.
One of the things we're currently discussing is post-market surveillance. We're in the process of looking at our guidelines, which are almost 15 years old, and if necessary, changing them to adapt to the modern environment.