Autoren

Dr. Bernd Renger is currently Vice President Quality Control at Vetter Pharma Fertigung in Ravensburg, Germany.
He holds a degree and a Ph.D. in Organic Chemistry from the University in Gießen, Germany.

1976 In 1976 he started his professional career with Hoechst AG as a R&D Chemist.

1984 After leaving Hoechst in 1984 he has held several management positions in Quality Control and/or Quality Assurance at Mundipharma (Limburg), Byk Gulden (later Altana Pharma, Singen) and Baxter BioScience (Vienna) before joining Vetter in 2004.

He is member of the Advisory Board of the European Compliance Academy and Chairman of the European Qualified Person Association, an organisation representing more than 1.300 Qualified Persons in Europe.

His main fields of interest are benchmarking and efficacy of quality operations, handling of deviations and OOS results, Quality Systems and role and responsibilities of the Qualified Person.

Publications at Maas & Peither GMP Publishing:

• GMP-MANUAL
  (Author of chapter 19.B The "Qualified Person" according to Directive 2001/83/EC)