Science Researcher Update: Spotlight on Meetings, Conferences, and Events

Webinar on Implementing an Internal Audit Program of QMA, Persisting to ISO 13485 & 21 CFR Part 820

Posted on Mar 7, 2015 6:47:00 AM

 
Seminar - Online
 
This webinar is intended to help you adequately develop an internal audit program of a firm's quality management system (QMS) as required by ISO 13485 or 21 CFR Part 820.
21 CFR 820.22 states "Each manufacturer shall establish procedures for quality audits and conduct such audits to assure that the quality system is in compliance with the established quality system requirements and to determine the effectiveness of the quality system."
Organization: Compliance Trainings (https://compliancetrainings.com)
For more information, please visit: http://bit.ly/1AmbH7p
 
Tuesday, 10 March, 2015  (13:00 - 14:00)
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Online
Phone: 4169154458
 
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Tags: Medical Device Technology, March, Webinar, Quality Control, 2015, Seminar

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