Autoren

1976-1980 Study of Chemistry / University of Wisconsin-Eau Claire (Eau Claire, Wisconsin, USA) / Bachelors of Science

1984-1989 Study of Pharmacology / University of Chicago (Chicago, Illinois, USA) / Doctorate

since 2005 Regulatory Affairs Certification (RAC) / Regulatory Affairs Professional Society (RAPS)

1980-1984 S.C. Johnson & Son, Inc. (USA), Product Development Chemist: Product development and technical support for surfactant based products

1989-1991 Northwestern University Medical School (USA), Postdoctoral Fellow: DNA sequencing

1991-1998 Abbott (USA) Research Biochemist/Technical Specialist/Senior Scientist: Product development and launch, technical support, validation, manufacturing and quality assurance for in vitro diagnostic products

since 1998 Abbott (USA) Regulatory Affairs Specialist/Program Manager Quality Operations: Regulatory submissions, advertising & promotional support, quality systems development, and auditing for a variety of product types including device, in vitro diagnostic, nutritional and animal health products

since 2005 Abbott Delegate to Clinical Laboratory Standards Institute (CLSI)

Publications at Maas & Peither GMP Publishing:

• GMP-MANUAL
  (Co-Author of Chapter 23 Medical Devices)
• GMP-BERATER
  (Co-Author of Chapter 23 Medizinprodukte)
• GMP-BERATER Paperback Band 12 Medizinprodukte