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