- TypeWebinar
- Location Fremont, California, United States
- Date 14-08-2018
Education/Teaching/Training/Development
Information Technology
Accounting/Financial/Banking/Insurance
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: [email protected]
161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA.
+1-800-447-9407