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Maas & Peither AG
Karlstrasse 2
79650 Schopfheim, Germany

Phone +49 (0)7622 666 86-70
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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:



Grad. in Civil Engineering Electric Engineering (Bingen Technical College and Kaiserslautern University)

since 1997 Boehringer Ingelheim Pharma GmbH & Co. KG with following special fields:

1997-1998 Computer Validation in pharmaceutical production (responsible for validation of automated production plants)

1998-2001 Head of various special projects in the field of data processing (e.g. introduction of a data collection system, securing supply to market during implementation of SAP R/3, millenium 2000 project) and expert responsibility for electrotechnical employees in pharmaceutical production

Head of Computer System Validation within Quality Operations Dept. (e.g. responsible for implementation of a harmonized quality assurance system for computer validation on a worldwide basis and implementation of 21 CFR Part 11 requirements)

2005 - 2009 Head of Training & Computer System Validation within Quality Operations Dept. (e.g. responsible for carrying out GxP-Training; also responsible for GxP compliant implementation and GxP compliant operation of superordinated computer systems)

2009 – 2010 Head of Group Systems & Governance within Supply Chain Management Dept. / BI Headquarter (e.g. responsible for Supply Chain Processes and the respective computerized systems used worldwide)

since 2010 Head of Group Computerized Systems, Validation & Compliance within Q & EHS / BI Headquarter (e.g. responsible for setting worldwide standards for Computer System Validation)

Publications at Maas & Peither GMP Publishing: