I'm going to work backwards on your question, Matt. It costs nothing in the facilities and does not require any consequential change to equipment, gas, whatever. So, that is a non-cost item. It does cost our customers and us working together. We have to re-validate the fact that the process, which uses oftentimes half the gas, that the traditional processes use, it does, we have to make sure we know we're using less gas so we don't have to validate that part of the question. We know there will be less ethylene, so we know that's not an issue. But, we also know the FDA pays particular attention to how much residual gas stays in the product. So, if it gets implanted into the patient, that's okay, but we know that's better, because we're starting out with less gas. So, all those things are known. We just need to be absolutely positively sure that we are sterilizing the device, when we do that, and that requires validation by the customers and us. We are working with it. It also currently or historically requires the agency to look at it and approve it. We are working with the agency to lay out templates to make that far simpler for our customers and far less of a regulatory burden for our customers to be able to do that. So, I'll call it the switching cost and switching cost is all around validation, than any other I'll call it material costs. Now obviously it uses a little less gas, that cost is largely immaterial in the process. So, as the Delta in the gas usage is relatively immaterial. And frankly, in most cases, our total cost is immaterial those are the transportation costs in the process. So, this is not a big cost issue. It is a get it right issue, and both we and our customers are very serious to make sure that in enhancing what's potentially the environment that we do not take any risks that the product is not sterile. Right now, we're, I'm going to use the world an oxymoron today in many cases. We're over sterilizing now. Once you kill all the bugs, you can't kill them again. So, we're over gassing and not really over sterilizing. And to the extent, we're over gassing, we don't need to do. It does, it takes time, but it's not measured in months for any specific customer to name a specific product. But there's a lot of customers and a lot of products up there. So, it will take STERIS years we believe. But, we do think and Mr. Carestio, our Chief Operating Officer who grew up in that business, absolutely believes and set a target for his team to get down 50%, using half the gas we used to use for the same level of requirements and do that inside of 5 years and we think we can hit those targets.