Wendy Kleijberg, EU QPPV studied Medicine at the Radboud University in Nijmegen and graduated as Master in medicine. She started her career in the pharmaceutical industry in pharmacovigilance in 2006 as local safety officer for a medium sized pharmaceutical company. After two years she continued her career at global pharmacovigilance level and started writing regulatory reports and performing signal detection. Due to a merger, she changed to a generic company and continued her activities on global level. After 8 years PV experience, she started a career as an independent consultant. She has been involved in many projects and PV systems. She is experienced in both local pharmacovigilance activities and global pharmacovigilance activities, from case processing to report writing, from local literature search to signal detection and from SOP writing to MedDRA subject matter expert. She is now acting as EU-QPPV for clients. She is working on various PV related projects, in line with company and client expectations, including but not limited to: LPPV expertise, global and local literature search, regulatory intelligence, case processing, report writing (RMP, PBRER), data analysis and signal detection activities, PV SOP writing, PSMF writing, etc.