Formulation Project Manager
Wendy has broad international experience working with start-ups to multinationals. She is a regulatory specialist, taking pharmaceutical candidates from non-clinical to market. Wendy was Licensing & Acquisition Manager at Lederle Laboratories and Regulatory Affairs Manager for Cyanamid's human pharmaceutical business where the focus was anti-infectives.
Formulation development & optimisation lead
Technical and Scientific Adviser
Stewart has worked in the pharmaceutical industry for approximately 50 years. He has occupied a number of senior management roles including Quality Assurance, Quality Control, Production, Validation and Logistics. A microbiologist by training, he spent 25 years of his career involved with sterile products ranging from standard pharmaceutical forms through vaccines to recombinant biotech products. He has spent the last 11 years as an independent consultant providing advice and training to both small and blue chip companies in the UK, Europe, USA and the Far East. He has acted as an expert for in excess of 50 license applications and has hosted numerous regulatory inspections throughout the world.