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:



PAT Implementation team leader, Process Analytical Sciences Group, Global Manufacturing Services, Pfizer

Seamus is an Analytical Chemist and studied at CIT in Cork Ireland.

He joined Pfizer in 1997 in an analytical role at the West Ryde plant in Australia. A year later he moved to an analytical role in the Technical Services group at the Pfizer Little Island drug substance plant in Cork, Ireland. In this role he was responsible for development and implementation of Process Analytical Technology at the site.

In 2003 he joined Pfizer’s global PAT support group (PASG) in a role focused on the development and implementation of new PAT technologies. He soon moved to the role of team leader of the PAT implementation team responsible for supporting sites in Ireland and Singapore. His role then expanded to team leader PAT implementation support for sites across Pfizer’s European manufacturing network. In his current role he leads a team that supports the implementation of PAT across all sites in Pfizer’s Primary Care/Oncology and Speciality/Biotechnology operating units. PAT is helping Pfizer to gain process understanding, reduce process variability and is enabling new manufacturing and quality paradigms such as continuous processing and real time release.

Prior to joining Pfizer Seamus held a number of roles in analytical development in Nycomed Amersham, Clonmel Healthcare and Glaxo Smithkline.

Publications at Maas& Peither GMP Publishing:
    (Co-author of chapter 20.D Process Analytical Technology (PAT))