Process Validation for Medical Device – Virtual Course

If you develop or manufacture medical devices, you need to be up-to-date on the latest regulations and requirements. Patients’ lives depend on it. This course covers the regulatory requirements for producing and distributing medical devices, including the requirements of 21CFR 820. We will discuss the background behind these regulations. We also address the systematic approach to evaluating and auditing the systems you need to meet the regulations. Take advantage of this opportunity discuss the validation of processes, facilities, utilities and compliance audits.

Please note: Registration is for one person only.

WEB-BASED

#652805 • September 25, 2008 • 8:00 a.m. – 4:00 p.m. Central

Member Price: $575 List/Forum/Division Price: $750

CEUs and ASQ RUs: 0.7

Instructor
James T. Schutta

Why Virtual?
ASQ Virtual Courses provide the same expert instructors, course materials and the ability to earn CEUs (and ASQ RUs) as our traditional educational courses, but they save you time away from work/family and save you money on lodging and other travel expenses. In short, they bring you all the training you need without all the hassle.