How can expected and regulatory requirements be met? How can quality and compliance be continuously ensured and improved in operational processes? How can the Qualified Person be integrated into a pharmaceutical quality system? Quality assurance is a systematic process that permeates the entire pharmaceutical company. It requires an appropriate organizational framework that ensures quality at the individual workplace as well as collaboration between departments and beyond company boundaries. This practical guide addresses the relevant areas and aspects of quality assurance in the pharmaceutical industry: quality assurance system, GMP compliance, supplier qualification, GMP-relevant contracts. Read about how to produce in compliance with the constantly changing GMP and FDA regulations.