Commissioning, Qualification and Validation Training Course :

Who Should Attend
Learning Objectives
Description
<strong>Course Schedule - 8-10 December 2008</strong><br/><br/>Because validation is the critical factor in achieving FDA approval of new and renovated facilities, it is essential that validated systems and equipment be commissioned using Good Engineering Practice (GEP) in a manner to facilitate the validation process.<br><br> This course will cover what has become the traditional approach to conduct Qualification and Validation, and will also show how that approach supports the new Regulatory Science and Risk Based Approach for the 21st Century. Current industry application of the impact assessment process for utility systems and equipment will be covered, and assessment results on Master Plans will be explained. The course demonstrates the importance of applying GEP in the preparation of design specifications, conducting design qualification, and correctly establishing contractor responsibilities for adherence to these specifications during construction and installation.<br><br> The course will show the relationship of all the steps in commissioning to the project life cycle. Necessary elements will be explored in detail to assure a successful integrated commissioning qualification effort. Examples will be used to provide guidance for development of sound commissioning and validation programs resulting in reduction of cost and time of 10-20%.
11/13/2008 To 01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Pharmaceutical
Course Category
Brochure Name
http://www.cfpa.com/PDF/2008/1954,C8-113,0812-205.pdf
Address
Amsterdam, The Netherlands Europe