Date :
Place : United States, Chicago
Contact Person:John Robinson
Description:
In this seminar, we will cover Design Controls for medical devices. We will understand the requirements for design controls and how to translate them into an efficient and effective process for your company. We'll cover the history, context, and requirements for design controls.Deadline for abstracts/proposals : 14th February 2017
Organized By :NetZealous DBA as GlobalCompliancePanel
Keynote Speakers : Susanne Manz Quality and Compliance Expert / Auditor for Medical Devices, Manz Consulting, Inc . 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 industry leaders like GE, J&J, and Medtronic, Susanne worked in various world-wide roles in
Conference Highlights :Overview: Design Controls are essential for producing safe and effective medical devices. And Design Controls are considered a critical process by the FDA. Yet, Design Controls are still one of the most frequent areas for 483 and Warning Letter observations. This 2 day seminar will help you understand, develop, and implement design controls processes and tools that are a competitive strength for your company. You will learn how to incorporate design controls into your product development proces
Venue :Chicago, IL, United States
Check the event website for more details.