The VP Regulatory Affairs is no longer listed as a position in the INSM website "Careers" section. My hope is that Lewis has filled this position, which will reasonably assure INSM capability to make future regulatory filings with FDA, EMEA and beyond. The money is there now that they off-loaded the "dead wood" from the company. Brian Richie should be tweeked to have INSM announce this hire, if it has been accomplished. The need for the manufacturing oversight person is less now that a cGMP contract manufacturer has been identified. If that CRO is passing cGMP product production for other companies, it is likely there will not be a need for parallel QC/QA. However, if they start a manufacturing site in Europe, they will need a cross trained person to work on that side of the pond.