Autoren

Study of pharmacy at the Technical University, Carolo Wilhelmina, in Braunschweig/Germany, Ph D thesis at the Institute for Pharmaceutical Biology of the Technical University
Specialized Pharmacist for Pharmaceutical Analysis
Authorized Expert for Control Tests according to § 65.4 AMG (German Medicines Act)

1994-1995 Planta Subtil Arzneimittel GmbH in Oldenburg/Germany:
Head of Laboratory in quality control department and marketing authorization

1995-1998 Solvay Pharmaceuticals GmbH in Neustadt/Germany:
Head of different laboratories in the quality control department, analysis of raw materials, bulk pharmaceuticals and medicinal products, control of packing materials, subcontractor management, subsequently Deputy Head of Quaity Control as well as Deputy Head of Quality Assurance

1999-2003 Wülfing Pharma GmbH in Gronau/Germany:
Head of Quality Control and in charge of medicinal product release for the market according to AMG (German Medicines Act)

since 2003 Labor L+S AG in Bad Bocklet-Großenbrach/Germany:
in January 2005, change-over to the Board of Directors of the Association, Technical Head of the Institution according to DIN EN ISO/IEC 17025 and, among other things, in charge of the Quality Management and Qualified Person since 2009

Consultant/author concerning several topics in the field of quality assurance and pharmaceutical analysis

Publications at Maas & Peither GMP Publishing:

• GMP-MANUAL
  (Author of chapter 17.B.4.1 Sample contract for contract analysis, chapter 17.B.6 Transfer of the test to the contract laboratory)