Design Controls are essential for producing safe and effective medical devices. And Design Controls are considered a critical process by the FDA. Yet is still one of the most frequent areas for 483 and Warning Letter observations. This 2 days seminar will help you understand and develop design controls processes and tools that are a competitive strength for your company. Intrinsic quality, safety, and effectiveness of a device are known to be established during the design phase. Yet, statistics show that a significant percentage of all medical device recalls are due to design problems. And design problems can have disastrous

Date : 5th October 2017 to 6th October 2017

Place : United States, Las vegas, nv

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901156SEMINAR?allconferencealerts-October-2017-SEO

Contact Person:Eevnt Manager

Description:

Design Controls are essential for producing safe and effective medical devices. And Design Controls are considered a critical process by the FDA. Yet is still one of the most frequent areas for 483 and Warning Letter observations. This 2 days seminar will help you understand and develop design controls processes and tools that are a competitive strength for your company. Intrinsic quality, safety, and effectiveness of a device are known to be established during the design phase. Yet, statistics show that a significant percentage of all medical device recalls are due to design problems. And design problems can have disastrous

Design Controls are essential for producing safe and effective medical devices. And Design Controls are considered a critical process by the FDA. Yet is still one of the most frequent areas for 483 and Warning Letter observations. This 2 days seminar will help you understand and develop design controls processes and tools that are a competitive strength for your company. Intrinsic quality, safety, and effectiveness of a device are known to be established during the design phase. Yet, statistics show that a significant percentage of all medical device recalls are due to design problems. And design problems can have disastrous will be held in Las vegas, nv,United States on date 2017-10-06

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Deadline for abstracts/proposals : 3rd October 2017

Keynote Speakers : Susanne Manz 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 C

Conference Highlights :R&D Engineers R&D Managers and Directors Individuals participating in Product Design and Development Individuals participating in design changes and failure investigations Regulatory Affairs Design Quality Engineers R&D engineers and scientists Compliance Specialists Auditors Senior Management

Venue :Las Vegas, NV, United States

Check the event website for more details.