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Key deadlines

Conference starts:

2018-03-08

Website

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Conference Description

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