Due to his broad experience he is familiar with German, European and FDA regulations for pharmaceuticals and medical devices.
Heinrich Prinz studied chemistry and genetics at the University of Cologne, Germany. He started his career in 1986 at Boehringer Mannheim where he was responsible for the implementation and validation of quality control methods for recombinant therapeutic proteins.
Five years later he joined Biotest AG as Head of Global Quality Assurance and concentrated his focus on quality management systems and combined systems for drugs, medical devices and In Vitro Diagnostics.
He is author or co-author of the following chapter of GMP Compliance Adviser: