Notice: Could not load module: 'blacklist' (required module files not found) in /kunden/228602_82418/webseiten/gmp/gmpupdate.swhosting6.de/modules/seitbox/SeitboxModule.php 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/gmpupdate.swhosting6.de/library/Seitbox/bootstrap.php on line 170
GMP Publishing - GMP/cGMP (current Good Manufacturing Practice)
  • gmp-verlag.de
  • 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
E-mail service@gmp-publishing.com

 

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
E-mail service@gmp-publishing.com

URL www.gmp-publishing.com

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!

Experts

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:

 

Author

Study of pharmacy at the Technical University, Carolo Wilhelmina, in Braunschweig/Germany, Ph D thesis at the Institute for Pharmaceutical Biology of the Technical University
Specialized Pharmacist for Pharmaceutical Analysis
Authorized Expert for Control Tests according to § 65.4 AMG (German Medicines Act)

1994-1995 Planta Subtil Arzneimittel GmbH in Oldenburg/Germany:
Head of Laboratory in quality control department and marketing authorization

1995-1998 Solvay Pharmaceuticals GmbH in Neustadt/Germany:
Head of different laboratories in the quality control department, analysis of raw materials, bulk pharmaceuticals and medicinal products, control of packing materials, subcontractor management, subsequently Deputy Head of Quaity Control as well as Deputy Head of Quality Assurance

1999-2003 Wülfing Pharma GmbH in Gronau/Germany:
Head of Quality Control and in charge of medicinal product release for the market according to AMG (German Medicines Act)

since 2003 Labor L+S AG in Bad Bocklet-Großenbrach/Germany:
in January 2005, change-over to the Board of Directors of the Association, Technical Head of the Institution according to DIN EN ISO/IEC 17025 and, among other things, in charge of the Quality Management and Qualified Person since 2009

Consultant/author concerning several topics in the field of quality assurance and pharmaceutical analysis

Publications at Maas & Peither GMP Publishing: