Collection of GMP's for pharmaceutical production
The GMP Handbook for pharmaceuticals
Quality Systems Handbook for MedDev
GMP translations (FR, IT, SE, DK)
Search tool and document library. Find you way in regulations, guides and other reference documents.
Dr. Harald Scheidecker is an engineer in biotechnology by education. He has 25 years experience in the pharmaceutical industry, mostly in quality assurance. He started in Research & Development at Schering AG, Berlin and Pharma Biotechnology Hanover working on genetic engineering.
After three years of international project management at Solvay, Hanover he headed the quality assurance department of Solvay´s pharmaceutical plant in Neustadt, Germany.
In 2001 he joints Boehringer Ingelheim as a corporate auditor for GMP compliance responsible for Boehringer Ingelheim manufacturing sites world wide and for contract manufactures. Since 2006 he held the position of an Associate Director GMP Auditing for the German Boehringer Ingelheim site. In this function he has extensive experience with national and international authority inspections by European, US and Asian inspectors.
In more than 120 national and international audits he execute audits by suppliers and contract manufactures for evaluating there GMP status and QA systems.
» Handling foreign inspections in a multicultural environment #5107
