MAR 15

How to Manage an effective FDA Inspection

   

Conference CFP

  

 

When:

  15 Mar 2017 through 15 Mar 2017

CFP Deadline:

  15 Mar 2017

Where:

  Online Event

Website URL:

  http://www.compliance4all.com/control/w_product/~product_id=501159LIVE?channel=mailer&camp=Webinar&AdGroup=brownwalker_Mar_2017_SEO

Sponsoring organization:

  Compliance4All

Categories:

  Medicine & Health > Other

Event description:

Overview: This webinar can help you be more professional and polished during an inspection. You will learn how to present information about your quality system in the most competent and professional manner. Why should you Attend: This webinar can help you prepare a strategy and detailed plan to more successfully prepare for, manage, and respond to an FDA or Notified Body Inspection. If you've had a recall, an increase in MDRs, or it's been more than 2 years since your last inspection, you can benefit from this webinar. Areas Covered in the Session: FDA Inspection basics Inspection preparedness strategy and planning Key roles during an inspection SME (Subject Matter Expert)training Checklists for preparing Who Will Benefit: Quality Engineers Compliance Specialists Compliance Managers Quality Managers 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. While at GE, J&J, and Medtronic, Susanne worked in various world-wide roles including Executive Business Consultant, WW Director of Quality Engineering and, Design Quality, and Director of Corporate Compliance. Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com

Posting date:

11 January 2017
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Placement:

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