Gudrun Bach
After studying pharmacy in 1986, Gudrun Bach worked in various pharmaceutical companies in drug production, specifically in quality assurance and the manufacturing of clinical trial materials as a Qualified Person. In May 1999, she transitioned to pharmaceutical supervision, initially at the district government in Neustadt/Weinstraße, and from January 2000 at the State Office for Social Affairs, Youth, and Supply, Pharmacy Branch in Mainz. There, she serves as an advisor in GMP (Good Manufacturing Practice) supervision of pharmaceutical and active ingredient manufacturers both domestically and abroad. Ms. Bach is the Quality Assurance Officer for the state of Rhineland-Palatinate and a member of the expert groups for quality assurance and inspections/evaluation systems/pre-approval at ZLG in Bonn. She is a specialist pharmacist for pharmaceutical technology.