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
1. Site Master File
A Sample for Download
according to PIC/S PE 008-4!
2. Checklist GMP-Inspections
650 questions typically asked during audits
3. Process Validation
official requirements, validation planning and procedure, ...
GMP Compliant Documentation
How to create, organize, review and archive GMP related documents in pharmaceutical industries
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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:
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Eisai, Inc., USA
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B&B Asesores, Spain
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Consultant, Germany
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Boehringer Ingelheim Pharma GmbH & Co. KG, Germany
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Consultant, Germany
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Maas & Peither AG, Germany
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F. Hoffmann-La Roche Ltd, Switzerland
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Labor L+S AG, Germany
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WDT eG, Germany
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Hecht Technologie GmbH, Germany
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Planttech Engineering GmbH, Germany
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Rottendorf Pharma GmbH, Germany
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GILYOS GmbH, Wuerzburg (Germany)
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Consultant, USA
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F. Hoffmann-La Roche Ltd, Switzerland
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Halfmann Goetsch Partner AG, Switzerland
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Chair of the Advisory Board
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Boehringer Ingelheim Pharma GmbH & Co. KG, Germany
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Ministry for Health of Land Schleswig-Holstein, Germany
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National Institute of Health Sciences, Japan
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Pharmaceutical Consultant, UK
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Orion Corp., Finland
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former Ecolab Engineering GmbH, Germany
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Swissmedic, Switzerland
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AstraZeneca, Sweden
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Basilea Pharmaceutica International Ltd., Switzerland
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phaRmaK-Beratung UG, Germany
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FDA Regulatory Compliance Consulting, USA
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Divisional Vice President, Strategic Regulatory Affairs
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Law Office Lücker MD-Law, Germany
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Maas & Peither AG, Germany
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Chair IPEC Europe Excipient Certification Committee
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Clarkston Consulting, USA
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Watson Pharamceuticals Inc., USA
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Bioscope Associates LLC, USA
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Pfizer Global Manufacturing, Ireland
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Pfizer Global Manufacturing, Ireland
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GMP Instructor, Germany
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Maas & Peither, Germany, USA
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Vetter Pharma Fertigung, Germany
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Sanofi-Aventis Pharma AG, Germany
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Merck KGaA, Germany
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comes compliance services, Germany
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F. Hoffmann-La Roche Ltd, Switzerland
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ProLeiT AG, Germany
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Bayer Schering Pharma AG, Germany
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Consultant, Switzerland
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PAREXEL Consulting, Uxbridge, Middlesex, England
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Fresenius Kabi AG, Germany
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Boehringer Ingelheim Pharma GmbH & Co. KG, Germany
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retired since August 2005 from Boehringer Ingelheim Pharma GmbH & Co. KG, Germany
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Health Canada
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Consultant, Germany
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Process Robustness Network, Germany
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Amgen, USA
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GxP Services, Germany
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Boehringer Ingelheim Pharma GmbH & Co. KG, Germany
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Associate Director Strategic Regulatory Affairs
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Karlstraße 2
79650 Schopfheim
Germany
E-Mail: service@gmp-verlag.de
Tel. +49 (0) 7622 6 66 86 70
Fax +49 (0) 7622 6 66 86 77
