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2018 - Design Control is Critical to Product Quality

Date2018-08-14

Deadline2018-08-12

VenueFremont, USA - United States USA - United States

KeywordsProduct Development Managers; Compliance Specialists; Design Quality Engineers

Websitehttp://www.compliance4all.com/control/w_...g_2018_SEO

Topics/Call fo Papers

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-AT-compliance4All.com

Last modified: 2018-06-14 15:32:56