Chris is a highly qualified quality and regulatory professional with a strong background in the medical devices, diagnostics, and pharmaceutical industries.

Chris joined CMR from Phillips RDT where he was Director of Quality Assurance and Regulatory Affairs and sat on the senior leadership team where he led the business through key regulatory milestones. Chris has also held senior quality and regulatory positions at Meridian Bioscience International where he was Vice President of Quality and Regulatory Affairs for the lifescience division.

At CMR, Chris will lead global regulatory strategy and execution, as well as overseeing quality assurance across the company’s products and services.