Ned and Sarah together have over thirty years’ experience in pharmaceutical and biotechnology
regulatory affairs with expertise in Australia, New Zealand and Europe. They are
experienced in working with and leading local and global project teams and interacting
with regulatory agencies.
Ned has been a regulatory affairs professional continuously
since 1997, working directly with Pfizer and other large pharma in both Regulatory
Development and Post-Marketing roles across EU, Australia and New Zealand markets.
Ned has been a Regulatory Consultant since 2006, when he first joined NDA Regulatory
Science in Leatherhead UK, Europe’s pre-eminent regulatory affairs specialty consultancy;
in this role, he serviced a breadth of large and small companies, across a wide range
of therapeutic areas and product types.
Ned qualified at the University of Melbourne
with both a BSc(Hons) in Pharmacology and a Graduate Diploma of Drug Development
and Pharmaceutical Science.
Sarah qualified with BSc(Hons) from the University of Sheffield and an MSc from the
University of Kent at Canterbury. She has specialised in Regulatory Affairs since
1999, where she started in Regulatory Development at Pfizer in Sandwich, Kent, UK,
working with European and International markets. After founding Greengage Regulatory
Ltd, UK, in 2011, specialising in EU Centralised Procedures, Sarah moved to Melbourne,
Australia, where she and Ned then together founded Greengage Regulatory Pty Ltd.