Dan is Senior Manager Regulatory Affairs & Quality Assurance at SFL. He leads regulatory and quality projects, providing strategic and operational advice to SFL clients for the development, filing, and maintenance of healthcare products such as medical devices, IVDs and combination products.

Dan’s experience over the past, nearly two decades, spans across Research & Development, Quality Assurance, and Regulatory Affairs on both the Manufacturer and Notified Body sides of the medical device world. His knowledge of regulatory requirements in global markets combined with his specialist experience in technical documentation is highly sought after by SFL clients.

Before joining SFL, Dan had worked in small, high pressure spin out companies as well as some leading medical technology companies. His most recent appointment prior to joining SFL, was as a Senior Product Specialist responsible for reviewing Class III medical devices under the MDR for a large Notified Body.

Dan has a Bachelor of Science in Chemistry, from Loughborough University, UK.