Medical Devices 2011 - Verification vs. Validation in Regulated Industries

Why Should You Attend:
Companies wishing to understand the risks and complications involved with the application of sound verification and validation principles will gain a better understanding of the differences and benefits by attending this training.

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?

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