That is correct, and it is because what Health Canada will approve is what is manufactured in Canada. In the last three or four weeks, companies in Canada in combination with our partners in Europe have been industrializing the design and have been securing the supply chain. It was necessary in some instances to wait until there was a signed contract in order for them to make commitments on such supply chains.
This week we have a complete device in Italy. We have the start of production of devices of a similar nature here in Canada. It will take us a few weeks to test them. Then that will be submitted to Health Canada, but in the meantime our discussions with Health Canada are to define what we should be testing and the complete set of tests that they will require, which in some cases means going slightly beyond what the FDA has asked for. They have been very helpful that way.