New professional society journal article reviews and illustrates the consequences of medical device risk management failures.
NATICK, MA – July 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, medical device product risk management, and regulatory affairs.
The article entitled “Understanding the Impact of Ineffective Medical Device Risk Management” is published in the July, 2010 edition of the Regulatory Affairs Professional Society journal Regulatory Affairs Focus.
The article addresses contemporary medical device product risk management practices for ensuring the safety of medical devices. It also identifies how risk management process can fail, and the negative consequences thereof.
The article is authored by Richard Morroney, RAC, CQA, Vice President, Quality & Regulatory Solutions, clinivation, Inc.
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