Description
<strong>Course Schedule - March 24, 2009 at 11:00 a.m. - 12:30 p.m. (EST) </strong><br/><br/>This 90-minute<b><i> accredited</b></i> online course is aligned with current industry “Risk-Based” initiatives and guidance provided in ICH Q9, ASTM E2500, and ISPE Baseline & Good Practice Guides. This course will provide insight on critical project decision making and enable a project team to identify and document data during the application of GEPs during the design, specification, and verification phases of a project. Discussions will focus on identifying and implementing Engineering Quality Systems to assure efficiency and quality.<br><br>
<b><u>Module 1:</u></b><br>
• GEP Overview<br>
• Engineering Quality Systems<br>
• GMP and GEP<br><br>
<b><u>Module 2:</u> </b><br>
• Design Review Process<br>
• Change Management<br>
• Risk Management<br><br>
<b><u>Module 3:</u> </b><br>
• Applying GEP to the Verification (Commissioning <br> & Qualification)<br>
• Integrating the Project and Engineering Lifecycles<br>
• Planning for Success<br><br>
<b>Question and Answer Session</b>
01/13/2009
To
01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Pharmaceutical
Course Category
Brochure Name
http://www.cfpa.com/PDF/2009/2284,C8-369,0903-410.pdf
Address
90 Minute Accredited Online Training Online Training