Sophie Trémeau is a Regulatory Affairs Specialist at BD Medical – Pharmaceutical Systems and provides guidance on the regulatory requirements to be considered for the design input specifications of new products. Mrs Trémeau also manages regulatory documentation to support BD’s biopharmaceutical partners in their drug-device combination product registration processes. She holds a biomedical engineering degree and, prior to joining BD in 2018, Mrs Trémeau worked for 10 years in operational quality and validation for a medical device company.