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Qserve opens a new office in Germany With the opening of a Qserve® office in Germany, a Qserve Group BV company with its headquarters in the Netherlands, the Qserve Group extends its global Regulatory compliance services for customers in Germany, Austria, Switzerland and Liechtenstein.  Read more...
Susanne Klymowsky promoted to Princinple Consultant at Qserve Consultancy Read more...
Workshop in Seoul, Korea titled, ‘International Trends of GMP Regulation and Inspection Practices for Medecal Devices On 25 June 2010, at the invitation of the Korean Food and Drug Administration (KFDA), Bill Greenrose, President of Qserve America, Inc., presented a workshop in Seoul, Korea titled, ‘International Trends of GMP Regulation and Inspection Practices for Medical Devices’ Read more...
Medical Devices Directive revision European Commission of Medical Devices. The Medical Devices Directive (MDD) 93/42/EG is revised on 21 March 2010. Read more...
Reclassification of joint replacements Commission Directive (2005/50/EC of 11 August 2005) reclassifying hip, knee and shoulder joint replacements comes into force in the Member States on 1 September 2007. Read more...
Medical Devices Exhibitions Agenda 2010 Read more...
Eudamed database obligatory by EU Member States from 1 May 2011. Europe’s long-awaited Medical Devices database is a reality Read more...
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