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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:




1994-1997 Institute for Pharmaceutical Chemistry, Münster

1998-1999 Galenical Dept., Rottendorf Pharma GmbH:
responsible for coordination of technology transfers, process optimisation

1999-2002 Production, Rottendorf Pharma GmbH
Head of Dosage Forming, Production manager

2002-2006 Pharmaceutical Technology, Rottendorf Pharma GmbH:
Head of Product Transfer, Process Validation

since 2006 Quality Assurance, Rottendorf Pharma GmbH:
Head of Quality Assurance, Qualified Person


Course Instructor for hygiene, QM-systems, supplier qualification, CAPA, auditing and inspections, change control, PQR, documentation, technology transfer, process validation, manufacturing technologies, packaging process, training sytems

Publications at Maas & Peither GMP Publishing:
    (Author of Chapters 11 Production, 13 Packaging, 15.C.2 Packaging instruction and batch packaging record, 18.E Self-inspection, 19.E Deviations, 19.G Product Quality Review and Annual Product Review)
  • Production - PDF Download
    GMP MANUAL Chapter 11 for Download
  • Preparing for the EU GMP Inspection - PDF Download