New professional society journal article reviews numerous, recent updates to the EU Medical Devices Directive.
NATICK, MA – September 1, 2010 – Clinivation, Inc. announced today the publication of a new professional society journal article coauthored by clinivation thought leaders in the areas of global market clearance operations and regulatory affairs.
The article entitled “Overview of EU Medical Devices Directive Updates” is published in the September, 2010 edition of the Regulatory Affairs Professional Society journal Regulatory Affairs Focus.
The article addresses numerous, recent updates to the EU Medical Devices Directive, including status and revisions to Directive 2007/47/EC, Essential Requirements, postmarket incidents, and conformity assessment procedures.
The article is authored by Richard Morroney, RAC, CQA, Vice President, Quality & Regulatory Solutions, clinivation, Inc.
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