Tuesday, August 14 | 10:00 am - 11:30 am
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