Quality Management Systems

Apr 25th, 2010
Following the success of our Medical Device Training Academy series, Medical Device Training days in 2009, we are once again providing a series of events under the Academy. Under the European Medical Device Directives, the most commonly used Conformity Assessment routes are based on the establishment, implementation, and maintenance of Quality Management Systems (QMS). This tutorial will explore in detail the issues surrounding the above, including experience gained to date and changes introduced by recent amendments to the Directive and Standards.
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