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."
Tuesday, 10 March, 2015 (13:00 - 14:00)
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Online
Email: suzzane.d@compliancetrainings.com
Phone: 4169154458
If you'd like to ask a question or post a comment about this talk please do so below.
This seminar posting is brought to you by Biotechnology Calendar, Inc. providing access to research information and research tools for nearly 20 years. Visit our Science Market Update Blog for current science funding and market information or see our schedule of upcoming science research laboratory product shows.