Mark started his career in manufacturing and has over 20 years’ experience in the pharmaceutical industry primarily as a Regulatory Affairs professional. Whilst he initially worked in Regulatory Affairs in Australia and New Zealand his scope has become global. In Auckland Mark had a Regulatory Affairs role with Schering AG. In Sydney, he continued his career working for companies including MSD, Novo Nordisk Pharmaceuticals. Having acted as a consultant and contractor, Mark brings diverse regulatory experience to GreenLight Clinical. Over the past 20 years, he has managed submissions in areas as diverse as medical devices, female health, radoopharmaceuticals, oncology, haematology, diabetes, cardiovascular, haemophilia, diagnostics, dermatology and andrology.