Autoren

1966-2007 Hoffmann-La Roche, Inc., Nutley, NJ USA

1981-2007 Roche liaison with the United States Pharmacopeia (USP) and member of Expert Committees, Advisory panels and Project teams.

1989-2007 Director of various departments within the Quality Management department responsible for Roche clinical and marketed pharmaceutical products, which included methods development, stability testing, analytical problem solving, methods validation, process and cleaning validation support, routine analyses, dissolution testing, product complaint evaluations, laboratory metrology services, and technical writing in a GMP compliant environment.

since 2007 Consultant in the area of Pharmaceutical Quality Management

Publications at Maas & Peither GMP Publishing:

• GMP-MANUAL
  (Co-author of Chapters 3 Premises, 4 Facilities and Equipment, 5 Pharmaceutical Water, 8 Cleaning Validation, 14 Laboratory and Analytical Controls and 15 Documentation)