Mr. Speaker, the largest criticism, both for research based pharmaceuticals and in fact for natural nutrients and products, has been that in the existing regime there is the capacity to back up in terms of applied research and getting the product onto the market.
I think this is in fact reverses that. A life cycle risk management is in fact a more dynamic process that places the onus on the full spectrum of medical jurisdictions, so to speak, and in fact will get those products out more quickly and in a safer manner. Surely that is the end result we all want to achieve. I think the legislation, properly worded and implemented, would do that.