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Contributed by dozens of experts from US, Europe and Japan. You get the best information when you need it.
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Maas & Peither AG
Karlstrasse 2
79650 Schopfheim, Germany

Phone +49 (0)7622 666 86-70
Fax     +49 (0)7622 666 86-77


Maas & Peither America, Inc.
1060 First Avenue, Suite 400
King of Prussia, PA 19406, USA

Phone +1 (610) 768-8028
Fax     +1 (610) 337-9548


TOP 5 GMP Downloads

1. Quality Agreement
Defines framework conditions and processes between contract givers and contract acceptors in order to meet mandatory quality criteria.


2. GDP Audit Checklist
More than 700 questions with reference to regulations for preparing and carrying out GDP audits.


3. GMP Audit Checklist
The GMP Audit Checklist works great for both sides - the auditor and the inspected company.


4. Technical Agreement
and Delimination of Pharmaceutical Responsibilities.


5. A Process Approach to Pharmaceutical Quality Systems
A Guide to ICH Q10 Compliance


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You need GMP information that is reviewed by GMP experts and is guaranteed reliable. Our advisory board includes members from US, Europe and Japan. They supervise the content and development of the GMP MANUAL. More than 50 experts around the world write articles that are peer-reviewed. You get the best GMP information when you need it.

Our panel has the right background and credentials to make sure that we provide the highest level of expertise and knowledge to the industry:




1990–1994 Study of pharmacy at University of Erlangen-Nürnberg ­(Germany)

1994-1995 Pharmacist in training for state examination

1996–1999 PhD thesis at University of Erlangen-Nürnberg (Institute of Pharm. Chemistry); R&D (medicinal/ pharmaceutical chemistry)

1999–2002 Public Pharmacy (Leadership)

since 2002 State Surveillance of Medicinal Products (Government of Free State of Bavaria, Germany); GMP-Inspector

since 2009 European Medicines Agency (EMA); GMP-Inspector


1998–1999 University Publications

since 2006 Lectureship at University of Erlangen-Nürnberg (“Pharmaceutical Legislation”)

2007-2013 Head of API-Group at Central GMP-/GCP-Surveillance Bavaria

since 2007 Board of Examiners 3. Pharmaceutical State Examination

since 2010 National and international lectures and publications related to GMP and pharm. legislation

since 2013 Head of national Expert Group EFG 2 “Inspections/GMP-Guidelines“

since 2013 Author Maas & Peither AG – GMP-Publishing

Publications at Maas & Peither GMP Publishing:
    (Author of chapter 21.A Introduction, 21.B Regulatory principles, 21.G Biotechnological active substances)