Live Webinar on
Verification vs. Validation in Regulated Industries
Date & Time:
Thursday, March 1, 2012 10:00 AM PST | 01:00 PM EST
Register Now
Duration: 60 Minutes Instructor: John Chapman
Location: Online Price : $245.00 (for one participant)
Instructor Profile:
Overview:
John Chapman
Attend this webinar to understand the differences and benefits of Regulatory Affairs
verification and validation. Learn about the risks and complications Professional,
involved with the application of sound verification and validation
principles. John Chapman, BS, MBA, RAC has
over 30 years medical device
regulatory experience and over 10
Why Should You Attend: years experience with the European
The meanings and regulatory requirements of the terms "verification" Union's medical device directive,
and "validation" are often confusing to engineers and even some 93/42/EEC. John has led two device
regulatory professionals. FDA regulations as well as European companies to ISO quality system
certification and CE marking. He has
standards such as ISO 13485:2003 require both verification &
been performed regulatory due
validation documentation throughout these regulations and
diligence on over a dozen
standards.The terms apply to design control, process control and acquisitions in the past 12 years,
others. Verification and validation also appear in the "essential exposing him to numerous quality
requirements" in MDD 93/42/EEC needed for CE marking medical systems, including consent decrees
devices in the European Union. Good engineering practices in all as well as many notified bodies. He
industries benefit from well executed verification and validation earned his regulatory affairs
studies. certification (RAC) in 1998 and was a
contributing author to 2004
Fundamentals of EU Regulatory
Areas Covered in the Session: Affairs, RAPS, 2004. ...more
l Verification & validation types
l Definitions Suggest a Topic More Webinars
l Design control
Your Necessity is our Priority
l Process control
l Application
l Consequences of poor verification & validation
l Why verification & validation makes good business sense
Click here to register for this webinar
Who Will Benefit:
l Quality & Regulatory Professionals
l Manufacturing & Design Engineers
l Marketing Product Managers
l Corporate & Operations Executives
It would be really nice if you can circulate this mail to all your deserving colleagues who can immensely
benefit from this program.
For more information, please contact the event coordinator. We look forward to seeing you at the webinar.
Best regards,
Event-coordinator
GlobalCompliancePanel
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