Andrew has an engineering doctorate in medical devices and is a talented and versatile consultant who has accumulated over 15 years’ experience in medical device and IVD design and development, regulatory affairs and quality systems, while holding a number of senior positions within a range of companies.

With a PhD in drug development and 10 years of post-doctoral research experience in chemistry and molecular biology, combined with 8 years’ manufacturing and consulting experience in the medical device regulatory and quality arena, Zennia contributes a strong set of regulatory and technical skills to the team.