Design Control is Critical to Product Quality
ENDED
Webinar by
Compliance4All
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On-Site
/ Webinar
USD 150.00
Details
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]
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]
Outline
Special Offer
One Dial-in One Attendee
Price: $150.00
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Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. .
Compliance4All has a panel of acclaimed Experts whose professional trainings help regulatory professionals and organizations in a number of ways and take them to their goal of meeting regulatory requirements. Compliance4All offers path breaking professional training solutions to organizations that help them address pain areas and overcome the challenges and difficulties associated with meeting regulatory requirements.
Compliance4All has a panel of acclaimed Experts whose professional trainings help regulatory professionals and organizations in a number of ways and take them to their goal of meeting regulatory requirements. Compliance4All offers path breaking professional training solutions to organizations that help them address pain areas and overcome the challenges and difficulties associated with meeting regulatory requirements.