Verification vs. Validation in Regulated Industries - Webinar By ComplianceOnline (Medical Device)
Venue: Online Event
|Event Date/Time: Apr 05, 2011||End Date/Time: Apr 05, 2011|
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 â€œverificationâ€ and â€œvalidationâ€ 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 â€œessential requirementsâ€ 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.
Consequences of poor verification & validation.
Why verification & validation makes good business sense?
Note: Use this promocode(117660) for 10% discount.