Dr. Christine Martin joined Abbott GmbH & Co. KG in 1999 - now AbbVie Deutschland GmbH & Co. KG - as a Manager Parenteral Formulation within the Global Pharmaceutical Research and Development Organization. In this position, she gained experience in the late phase development of Humira® Pre-filled Syringe and Humira® Pen. In 2009, she then moved to Clinical Supplies Operations, heading a group for the manufacture of clinical supplies for oral dosage forms. Since 2012, she is leading a section within Clinical Supplies Operations Parenterals, dealing with Material Management, CAPA / Compliance, Visual Inspection and Batch Records. Christine Martin studied Pharmacy at the Albert-Ludwigs-University in Freiburg (Germany). She completed her Ph.D. in 1999 in a cooperation with Roche Diagnostics and the Department of Pharmaceutical Technology at the Albert-Ludwigs-University, Freiburg.