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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.

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1990-1992 Boehringer Ingelheim GmbH Corporate Division Quality Assurance: Compliation of Manuals and Guidelines for the Corporation on various topics relevant to GMP

1993-1994 Boehringer Ingelheim KG
Pharmaceutical Production Dept.;
Head of GMP: Qualification, Validation, SOP System, Manufacturing Documentation, Self-Inspection, Prepration for PAI, IT Projects

1994-1995 Boehringer Ingelheim KG
Pharmaceutical Production Dept.;
Head of Production of Granules/Tablets/Micronisation

1995-2002 Boehringer Ingelheim Pharma GmbH & Co. KG
Drug Delivery Department;
Head of Process Development/Investigational Supplies:
Process Optimisation, Scale-up, Product/Technology Transfer from R&D to Production; Manufacturing, Packaging and Labeling of Investigational Supplies

since 2002 Vice President Drug Delivery Department

Publications at Maas & Peither GMP Publishing:
    (Author of chapter 15.D Standard operating procedures (SOPs))