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From GlobalCompliancePanel
Interfacing Design Verification Process Validation and Design Validation - Webinar GlobalCompliancePanel
Overview: There is confusion between the requirements for Design Verification, Process Validation and Design Validation. While each of these processes has its own requirements, they do not stand alone, they are linked together. As this linkage is not well understood, it is the source of FDA observations and potential release of products that do not meet requirements.
Tuesday, March 13, 2012
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Risk Management in IEC 60601-1 Third Edition
...r will be on March 23, 2010. Webinar will be presented by Edwin L Bills.
IEC 60601-1 Third Edition was released in late 2005. It is a new philosophy in standards for medical electrical devices to accommodate rapid advances in technology. This new philosophy has been difficult for test houses and compliance bodies to absorb and develop test strategies. Currently, the EU and Canada have
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Business, Project and Compliance Risk
GlobalCompliancePanel brings a new webinar on the topic of Business, Project and Compliance Risk.
Webinar will be on March 2, 2010. Webinar will be presented by Edwin L Bills. Mr. Bills has held a number of quality and regulatory affairs positions. Mr. Bills is ASQ Certified as Quality Engineer, Quality Auditor, and as Manager of Quality/ Organizational Improvement.
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