Process Validation for the Pharmaceutical and Medical Device Industries Training Course :

Who Should Attend
Learning Objectives
Description
<strong>Course Schedule - May 14-15, 2009</strong><br/><br/>Validation of manufacturing processes in the cGMP environment is recognized by the medical manufacturing industries and by the regulatory agencies in the U.S., E.U. and Japan. This course will give the attendee an overview and understanding of the validation process, how to organize it and carry out process validations, key areas to look for during an audit, and assist managers in overall planning.<br><br> Various approaches to validation will be discussed with actual examples of successes and failures of industry validation experiences.<br><br> <b>Participants are invited to bring examples of their own validation issues to be discussed during the case studies session.</b>
01/13/2009 To 01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Medical Device
Course Category
Brochure Name
http://www.cfpa.com/PDF/2009/0736,C8-196,0905-301.pdf
Address
Burlingame, CA USA