That is an excellent point. What happens many times is the project is broken up into sections. There’s a general product development project, and then several separate regulatory projects hooked onto it, one for each country or region. You will often see a medical device come onto the market at different times in each country due to the differing requirements. Some countries, for example, would require more testing than others, so that takes extra time. We learn more about this next semester in Advanced Medical Device Development.