A qualified pharmacist, Ms Ström worked for a short time in retail pharmacy before an appointment in clinical research and regulatory affairs for Solvay BV in the Netherlands. Since then, Denise has worked at a senior level for both pharmaceutical companies and regulatory consultants. She joined CM&D from Sinclair Pharmaceuticals, where she was Director of Regulatory Affairs, with responsibilities including pharmacovigilance, medical information and reimbursement. Ms Ström is an active member of both the Royal Pharmaceutical Society of Great Britain and The Organisation for Professionals in Regulatory Affairs (TOPRA). She has a depth of experience in both the USA and Europe, including clinical trial protocols, regulatory applications and expert reports across a broad range of therapeutic classes.