Fiona Cameron

​Fiona serves the Vice President of Regulatory Affairs for Meissa Vaccines. She has more than 24 years of experience in managing the regulatory process for biopharmaceuticals, in particular for vaccines. Previously, Fiona was Director of Regulatory Affairs, Oncology at Genentech and Senior Director of Regulatory Affairs at VaxGen. Since 2006, she has worked as an independent regulatory affairs professional leading regulatory activities for vaccine and biopharmaceutical companies. She has extensive experience with live viral and bacterial vaccine programs including cholera, anthrax, typhoid, RSV, HIV, smallpox, and influenza vaccines at the pre-IND, IND/CTA, NDA/BLA/MAA, and post-marketing stages. Over the last year, Fiona has led and executed two pre-IND packages for FDA, including a vectored RSV vaccine candidate, and filed one IND and one License Application. She has a B.Sc. in biology from University College, London.