Notice: Could not load module: 'blacklist' (required module files not found) in /kunden/228602_82418/webseiten/gmp/ on line 700

Warning: Warning: output buffer is not empty, but dispatching and rendering content has not been started yet. in /kunden/228602_82418/webseiten/gmp/ on line 170
GMP Publishing - GMP/cGMP (current Good Manufacturing Practice)
  • GMP MANUAL Login
  • Shopping cart

#9 Reliable peer-reviewed information

Contributed by dozens of experts from US, Europe and Japan. You get the best information when you need it.
Contact us

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


Your benefits:

> no shipping costs
> no waiting period: if you choose payment by credit card you will receive an email with the download information immediately after payment.


>>> Click here to find more Downloads!


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:



1996-2001 Biological Process Engineering (Fachhochschule Hannover)

2001-2002 WDT eG: Cooperation on reorganization of sterile areas. Key area: Qualification of facilities and equipment. Compilation of VMPs and SOPs.

2002-2004 WDT eG: Qualification Manager for rooms and facilities. Key area: Qualification of high-purity water systems and distribution systems. Cleaning Validation Manager. Planning and controlling of maintenance, calibration and requalification of GMP-relevant facilities and equipment. Project Coordinator: Reconstruction of a weighing centre according to GMP.

2004-2006 WDT eG: Additionally, coordinator of various projects in the area of industrial engineering: Energy monitoring, improvement of infrastructure in the area of steam production, heating and cooling, as well as their distribution. Reconstruction of a laboratory ventilation system. Construction, implementation and qualification of a building control system according to GMP.

since 2006 WDT eG: Head of engineering, qualification, cleaning validation, clean room ventilation, calibration, monitoring systems (production and storage), maintenance and servicing. Project Manager for con-version and new building projects in the area of manufacturing and production technology.

since 2009 Member of the International Association for Pharmaceutical Technology

since 2009 Member of the Association of German Engineers (VDI)

Publications at Maas & Peither GMP Publishing: