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Richard M. Bonner
Formerly with Eli Lilly, United Kingdom
Mr Bonner is currently located in the UK and works as a consultant to the Pharmaceutical Industry. Previous to his current role he was a Senior Quality Adviser for Eli Lilly and Company. He had 31 years experience within the pharmaceutical industry working in production, technical services and both Quality Control and Quality Assurance functions. He has been involved in multiple inspections from the MHRA, FDA and other authorities. Mr Bonner is a Qualified Person in Europe. He is now Associate Partner with Concept Heidelberg.
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Alfred Keusch
Baxter AG, Vienna, Austria
Alfred Keusch is an engineer and business manager and since 1990 responsible for the centralised purchasing at Baxter AG in Austria. Since 2000 he is Director Strategy & Operations for the Global Category Management and the procurement for the European sites of the division BioScience.
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Diana Eifler
F. Hoffmann-La Roche AG, Basle, Switzerland
In 2000, after gaining experiences in different industries locally and abroad, Ms Eifler joined F. Hoffmann-La Roche AG, Basel. Up to now, she is responsible in the logistic center at Roche for supply of different FDA relevant printed packaging-, marking- and auxiliary materials. Finally, she earned the CPIM designation (APICS) and gives lectures at the University of Cooperative Education, relative to the topics SCM, enterprise resource planning, logistics and e-procurement. |
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Karl Metzger
Welding GmbH & Co. KG, Hamburg, Germany
After several years experience in different GMP projects in chemical and pharmaceutical industry, Karl Metzger joined Weldings‘s QM&RA unit in 2001. There his focus is on Weldings‘s Integrated Management System, GMP projects, audits, warehousing. Currently he is a member of FECC‘s GTDP (Good Trade and Distribution Practice) Committee. Furthermore he is an APIC certified ICH Q7a Auditor.
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Prof Dr Claus W. Gerberich
Prof Gerberich & Partner International Consultancy, Germany
Professor Gerberich is managing partner of the consultancy. He studied mechanical engineering and business management in Mannheim, Karlsruhe and at the MIT in Cambridge. He worked 24 years in the industry, including 16 years as a board member of Schöller Lebensmittel, adidas AG, Batelle Europe, and finally Staff Leuchten.
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John Taylor
Medicines & Healthcare Products Regulatory Agency (MHRA), London, United Kingdom
John Taylor is Quality and Standards Manager Acting and Group Manager, Enforcement and Intelligence of the UK Medicines and Healthcare Products Regulatory Agency. Mr Taylor is currently responsible for all quality matters within the Inspection and Enforcement Division. He is a Chartered Chemist, a Fellow of the Royal Society of Chemistry and a member of the British Institute of Regulatory Affairs.
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