Claudia Mueller

Claudia Mueller, PhD, is currently working as a Biologics Quality Assessor in the Sector of Medicinal Product Authorisation and Vigilance of Swissmedic, the Swiss Agency for Therapeutic Products in Berne, Switzerland. Before joining Swissmedic, she was working as Associate Director and Head of a Formulation Development Team within Lonza Parenteral Drug Product Services at Basel. Previously, she was a Principal Scientist, Pharmaceutical Development at F. Hoffmann-La Roche Ltd. and a Senior Scientist at Novartis Pharma AG. Her expertise covers, amongst others, large and small molecule parenteral drug product development including formulation and manufacturing process development for early- to late-phase and commercial products, process characterization and validation (PC/PV), quality-by-design, technology transfer to commercial production, support for clinical and commercial drug product manufacturing, and regulatory submissions (initial authorizations & post-marketing submissions). She is author and co-author of various publications and book chapters in the field.