Conference - Online
We will discuss how Risk Management Files are developed and maintained in accordance with ISO 14971 throughout the product lifecycle.
Overview of ISO 14971 Medical devices - Application of risk management to medical devices
Discussion of key requirements
What written procedures and training are required
How to develop Risk Management Files
How to apply Risk Management to Post-Approval Labeling Risk Management Strategy
Understanding of what auditors expect
Speaker: Peter Spath
Organization: Global Compliance Trainings
For more information, please visit: http://www.globalcompliancetrainings.com/index.php?route=product/product&product_id=11&list=Peter%20Spath
May 25, 2014 - May 25, 2014 (10:00AM - 01:00PM)
201, N Squirrel road, Suite 1007, Auburn Hills, Michigan United States - 48326
Contact: John Gordan (webinar@globalcompliancetrainings.com)
Phone: 2482120588
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