How to Manage an effective FDA Inspection

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Category Compliance Specialists, Compliance Managers, Quality Managers

Deadline: March 14, 2017 | Date: March 15, 2017

Venue/Country: Online Event, U.S.A

Updated: 2017-01-16 20:32:46 (GMT+9)

Call For Papers - CFP

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: supportcompliance4All.com