Robyn Cochrane

With experience in both global medical device manufacture and start-up environments, Robyn offers a key understanding of the quality, regulatory and clinical requirements during new product development and introduction to the market of innovative technologies. Robyn has been responsible for driving regulatory strategy and ensuring a high level of organisational compliance to both national and international legislation. Through submissions to several regulatory agencies, she has facilitated the conduct of vital pre-market clinical work and subsequently achieved new device clearances in both the United States and European territories.

Robyn holds a Bachelor’s degree in Immunology & Microbiology and has experience within the orthopaedics, cardiology and sports medicine sectors.