Effective Risk Management & Quality System Implementation for Medical Devices
Webinar - Online
This course will provide attendees with a broad understanding of the quality management system requirements outlined in the recently-updated medical device standard EN ISO 13485:2012 and 21 CFR 820. The course focuses on teaching the process approach for quality management and how EN ISO 13485:2012, EN ISO 14971:2012 (Risk Management Standard) and FDA’s Quality System Requirements complement each other.
This 90 minute training is valuable tool for any organization having to demonstrate its ability to provide medical devices that consistently meet customer and regulatory requirements, while serving as a guide to develop and maintain a robust quality system. Participants will have an opportunity to learn about industry best practices and common pitfalls to avoid when implementing or maintaining a quality system.
Organization: Life Science Training Institute
(Courtesy of Life Science Training Institute's logo, via lifesciencetraininginstitute.com)
Effective Risk Management & Quality System Implementation for Medical Devices
Tue, Oct 29, 2013 - Tue, Oct 29, 2013 - 01:00 to 02:30 (GMT-05:00) Eastern Time (US & Canada)
Online
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