An Introduction to Process Validation - Webinar By ComplianceOnline (Medical Devices)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Jun 20, 2012 End Date/Time: Jun 20, 2012
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This webinar will cover the basics of process validation for pharmaceutical products and give you a strong understanding of what is involved. It will provide beginners an understanding of the validation master plan, validation protocols, IQ, OQ, PQ and types of validation.

Why Should You Attend:

With new manufacturing technologies increasingly becoming a larger part of our pharmaceutical product supply, validation is gaining in importance to pharmaceutical manufacturers. Whether a firm performs its own validation, hires a validation contractor or delegates the responsibility to a third party contract manufacturer, the ultimate responsibility always falls to the firm whose name appears on the label. The only way that this can be done with confidence is to have an adequate number of validation experts on staff. Since many firms believe that they no longer need an in-house validation staff, they have done away with this overhead cost. Now it is essential to have a minimal on-site validation presence. Since there are very few validation experts today. It is often necessary to train people in this lost art.


Online Event
2600 E. Bayshore Road
Palo Alto
United States