2012 - Verification vs. Validation in Regulated Industries - Webinar By GlobalCompliancePanel

Overview: Attend this webinar to understand the differences and benefits of verification and validation. Learn about the risks and complications involved with the application of sound verification and validation principles.

Why Should You Attend: The meanings and regulatory requirements of the terms "verification" and "validation" are often confusing to engineers and even some regulatory professionals. FDA regulations as well as European standards such as ISO 13485:2003 require both verification & validation documentation throughout these regulations and standards.The terms apply to design control, process control and others. Verification and validation also appear in the "essential requirements" in MDD 93/42/EEC needed for CE marking medical devices in the European Union. Good engineering practices in all industries benefit from well executed verification and validation studies.

Areas Covered in the Seminar:
Verification & validation types
Definitions
Design control
Process control
Application
Consequences of poor verification & validation
Why verification & validation makes good business sense
Who Will Benefit: Employees who will benefit include:
Quality & Regulatory Professionals
Manufacturing & Design Engineers
Marketing Product Managers
Corporate & Operations Executives

Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com

Phone: 800-447-9407
Fax: 302-288-6884