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March 08
conference-meeting
Mar 8, 2018
Credits:

Overview: You'll learn how to identify, segregate, control, and disposition non-conforming material. You'll learn about conducting failure investigations and requirements for correction and corrective action. Why should you Attend: Dealing with non-conforming material is a necessary process for medical device manufacturers. Yet, non-conforming material is a top reason for 483 and Warning letter citations. Areas Covered in the Session: Overview of the Regulations Definitions and Expectations Segregation and Control Disposition of NC material Concessions Who Will Benefit: Quality Systems Specialists Document Control Specialists Quality and Compliance Specialists Internal Auditors and Managers Quality Engineers Speaker Profile: Susanne Manz MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities. Event Fee: One Dial-in One Attendee Price: US$150.00 Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com

Member Price: 150.00 Non Member Price:

Contact Information

Event Manager Netzealous LLC DBA - Compliance4All 161 Mission Falls Lane, Suite 216, Fremont, CA 94539 United States of America 18004479407 (Tel) 302-288-6884 (Fax) support@compliance4All.com