Verification vs. Validation in Regulated Industries - Webinar By GlobalCompliancePanel

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@globalcompliancepanel.com http://www.globalcompliancepanel.com   Phone: 800-447-9407 Fax: 302-288-6884