Essentials of Dealing with Non-Conforming Material

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Category Non-Conforming Material, Medical Webinars, Quality and Compliance Specialists, Manufacturing Managers, CAPA Specialists, fmea for medical devices

Deadline: March 07, 2018 | Date: March 08, 2018

Venue/Country: Online, U.S.A

Updated: 2018-01-30 16:15:31 (GMT+9)

Call For Papers - CFP

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: supportcompliance4All.com