Triona is a highly experienced leader of Regulatory, Clinical and Quality with extensive experience in developing medical device quality systems, regulatory and clinical strategies. She also has vast experience in product development, design assurance, manufacturing and supply chain operations. She has a track record of getting medical devices from design concept to fully approved in both the US and Europe.   Triona holds a BSc in Polymer Engineering and a MSc in Medical Device Technology Regulatory Affairs. Previously she has held senior management roles in the pharmaceutical, food packaging, environmental and plastic packaging industries.