The department that's responsible for the medical device establishment licence is one department, whereas the MDSAP quality audit system is under the medical devices bureau as opposed to the inspectorate, so there are two departments. We're currently working on a proposal to bring to Health Canada to show them how similar these audits are and to see whether there's a way that it can realistically be addressed. We're in the process of putting that together.
On February 7th, 2019. See this statement in context.