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Maas & Peither AG
Karlstrasse 2
79650 Schopfheim, Germany

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



1976-1980 Study of Chemistry / University of Wisconsin-Eau Claire (Eau Claire, Wisconsin, USA) / Bachelors of Science

1984-1989 Study of Pharmacology / University of Chicago (Chicago, Illinois, USA) / Doctorate

since 2005 Regulatory Affairs Certification (RAC) / Regulatory Affairs Professional Society (RAPS)

1980-1984 S.C. Johnson & Son, Inc. (USA), Product Development Chemist: Product development and technical support for surfactant based products

1989-1991 Northwestern University Medical School (USA), Postdoctoral Fellow: DNA sequencing

1991-1998 Abbott (USA) Research Biochemist/Technical Specialist/Senior Scientist: Product development and launch, technical support, validation, manufacturing and quality assurance for in vitro diagnostic products

since 1998 Abbott (USA) Regulatory Affairs Specialist/Program Manager Quality Operations: Regulatory submissions, advertising & promotional support, quality systems development, and auditing for a variety of product types including device, in vitro diagnostic, nutritional and animal health products

since 2005 Abbott Delegate to Clinical Laboratory Standards Institute (CLSI)

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