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Laboratory and scientific exhibitions and conferences
News Release from: Institute of Validation Technology | Subject: Equipment Qualification and System Validation
Edited by the Laboratorytalk Editorial
Team on 02 November 2006
Equipment qualification and system
validation
This annual conference for pharmaceutical and biotechnology companies and will be taking place 5-7 December 2006 at Dorint Sofitel Amsterdam Airport Hotel, Amsterdam, Netherlands
This one-of-a-kind equipment qualification event will be lead by a team of industry experts who will take you through the equipment qualification and system validation process from beginning to end The learning process will include DQ (design qualification), IQ (installation qualification), OQ (operational qualification), PQ (performance qualification), and AIQ (analytical instrument qualification)
This article was originally published on Laboratorytalk on 31 Aug 2005 at 8.00am (UK)
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Then attendees will apply equipment qualification techniques they've learned throughout the conference with exclusive hands-on training in the local laboratory of a major industry equipment supplier - Dionex.
Speakers include:.
Malcolm Olver, GMP inspector, MHRA.
Hans Martens, computer system auditor, Eli Lilly.
Ludwig Huber, compliance programme manager, Agilent Technologies.
Carolyn Stockdale, associate director of IT, Millennium Pharmaceuticals.
Jim Hains, Manager, laboratory compliance and logistics, Berlex Laboratories.
Charlie Sodano, manager information services, Berlex Biosciences.
Bryan Hunt, lab operations manager, Sandoz.
Karl Fitt, analytical manager, chemical and pharma development, Evotec (UK) .
Stephen Luke, business development manager, NLG Analytical .
Felicia Ford-Rice, senior director, quality assurance, Astellas Pharma US.
Paul St Jean, product manager, global compliance programmes, Waters.
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