Essentials of Dealing with Non-Conforming Material

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: [email protected]

Others Details

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