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Design Control is Critical to Product Quality

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Website http://www.compliance4all.com/control/w_product/~product_id=502015LIVE?channel=ourglocal_Aug_2018_SE | Edit Freely

Category Design Control Basics, Quality Trainings, Design Control Process, Quality System Requirements, Product Development Managers, closed loop system

Deadline: August 12, 2018 | Date: August 14, 2018

Venue/Country: Online, U.S.A

Updated: 2018-06-07 14:32:52 (GMT+9)

Call For Papers - CFP

Overview:

This 90-minute webinar will cover the basics of design controls for

medical devices. Design Controls are an integrated set of

management practices that are customer focused and ensure

quality and consistency.

Why should you Attend:

Design Control is not only a regulatory requirement, it is a set of

aligned practices that deliver a rigorous, methodical, and

predictable design process leading to better product development

projects and more successful products.

Areas Covered in the Session:

Overview and Definitions

FDA Expectations, Regulations

Design Control Process

Planning

Design Inputs

Design Outputs

Who Will Benefit:

R&D Engineers

R&D Managers and Directors

Product Development Managers

Individuals participating in Product Design and Development

Individuals participating in design changes and failure

investigations

Regulatory Affairs

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.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: support@compliance4All.com


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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