CAPA within a Device Quality System - 2017

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Category CAPA Process, Device Quality System, Medical Device Companies, How to structure your CAPA process, How to use IT tools, Compliance courses on CAPA, Quality System requirements, medical device industry

Deadline: August 08, 2017 | Date: August 09, 2017

Venue/Country: Online, U.S.A

Updated: 2017-06-15 15:12:39 (GMT+9)

Call For Papers - CFP

You’ll learn how to streamline and monitor your process to ensure

compliance and improved performance. If your CAPA process needs a CAPA

this webinar is for you.

Why should you Attend:

Corrective and Preventive Action (CAPA) is the cornerstone of a strong

Quality Management System. And yet, many medical device manufacturers

struggle to establish and maintain and effective CAPA process.

Areas Covered in the Session:

FDA and NB expectations for CAPA

Lessons Learned from 483s and warning letters

Common problems CAPA

How to structure your CAPA process

How to use IT tools to monitor and maintain your CAPAs

Metrics to ensure your CAPAs are timely and effective

A toolkit for CAPA

Best Practices

Who Will Benefit:

Quality Systems Specialists

Document Control Specialists

Quality and Compliance Specialists

Internal Auditors and Managers

Training Specialists

CAPA Specialists

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.

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: supportcompliance4All.com