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#9 Reliable peer-reviewed information

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:



Pharmacist (University of Mainz, Germany)

1985–1990 Studies of pharmacy,
University of Mainz

1991–1994 Doctoral thesis, Institute of Pharmaceutical Biology, University of Heidelberg

1995–1996 GEHE Medica GmbH, Göttingen and Weimar:
Customer consultancy for pharmaceutical contract manufacturing

1997–1998 EPA Euro Pharma GmbH, Kronberg/Taunus:
Project Manager Regulatory Affairs

1999–2001 Alpharma-ISIS GmbH, Langenfeld:
Manager Business Development

since 2001 kohlpharma GmbH, Merzig:
Head of Quality Assurance and Qualified Person, Responsible for QA-, GMP-, GDP- and Cool Chain-Processes, Risk Management, Qualification and Validation, Auditing

since 2008 kohlpharma GmbH, Merzig:
in addition: Head of Pharmaceutical Development

Publications at Maas & Peither GMP Publishing: