Quality System 2017 - Managing an FDA Inspection

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-AT-compliance4All.com