Autoren

Pharmacist

since 1991 he has worked for the State of Schleswig-Holstein (Germany) in Drug Control, as Head of the Laboratory for Drug Analysis and later as GMP Inspector for the Regional Authorities for Health and Occupational Safety of the State of Schleswig-Holstein.

since May 2005 he has been working within the Ministry for Social Affairs, Health, Family, Youth and Senior Citizens, responsible e.g. for supervision of drug surveillance.
Member of the expert group on "Qualification/Validation" (1998-2008 head of the expert group).

He is also active in international committees, among other things as expert for the EMEA and the International Conference on Harmonization (ICH).

Publications at Maas & Peither GMP Publishing:

• GMP-MANUAL
  (Author of Chapters 2.A Place of work and job descriptions to 2.D Function owners subject to public law, 3.A Official requirements, 6.A Official requirements, 7.A Official requirements, 7.I Quality by Design / Kapitel 7.J Process Analytical Technology (PAT), 8.A Official requirements, 14.J Batch release, 15.A Official requirements, 17.A.8 Framework contract for contract manufacture and quality control, 18 Inspections (Kapitel 18.A Principles to 18.D Organization of inspections, 18.F Inspection of contract manufacturers and 18.G Inspection of suppliers) and 19.C Change control)