What you Need to Know to Prepare FDA Inspection

MessageThis Webinar is over
Date Aug 30, 2018
Time 10:00 AM to 11:30 AM
Cost $ 150.00
Although an effective Quality System should always be inspection 

ready, many medical device companies make basic mistakes 

during inspections leading to 483s and even warning letters. This 

webinar can help you manage inspections efficiently and 


Why should you Attend:
This webinar can help you prepare a strategy and detailed plans 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. 

Who Will Benefit:
Quality Engineers
Compliance Specialists
Compliance Managers and Directors
Quality Managers and Directors
Consultants and Contractors

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. Susanne has a BS in Biomedical Engineering and an 

MBA from the University of NM.  

Event Fee: One Dial-in One Attendee Price: US $150.00

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


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