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Managing an FDA Inspection

 
  January 04, 2017  
     
 
Compliance4All, Online
2017-03-15


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
 
 
Organized by: Compliance4All
Invited Speakers:
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.
 
Deadline for Abstracts: 2017-03-14
 
Registration:
Contact Detail:

Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
E-mail: support@compliance4All.com
 
   
 
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