Dr Tamsin Dawson is a biologicals regulatory affairs consultant for the animal health industry in the EU. The company she represents, Triveritas (a contract research organisation), supports academia and new start-up companies to SME and large biopharmaceutical companies with the regulatory and clinical provision they require to develop and register veterinary medicines in the EU and US. This includes the maintenance of successful registrations. Tamsin specifically provides regulatory support for veterinary biologicals (vaccines, serum products etc) and has 13 years regulatory experience.
Tamsin worked in industry for a SME pharmaceutical company, prior to moving to Triveritas in 2009. This work saw Tamsin heavily involved in a knowledge transfer partnership between an academic partner and the industrial partner. During this time, Tamsin was responsible for developing and validating immunological assays for quality control testing of a veterinary biological, establishing a QC laboratory on-site at the industrial partner, and supporting on regulatory asects (dossier writing, stability testing etc) for two product marketing authorisations.