What you Need to Know to Prepare FDA Inspection

Overview:
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
effectively.

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: [email protected]