Description
<strong>Course Schedule - 23-25 February 2009</strong><br/><br/>From both a regulatory and business perspective, firms
should partner with their suppliers (both vendors and contract
suppliers) to assure that they receive materials and services
according to predetermined specifications for quality, quantity
and delivery. Some firms limit this activity to some degree of
“qualification” while others extend it to “certification” or to
some type of “strategic alliance.”<br><br>
This course reviews the regulatory, legal and operational
aspects including the role of the quality and operations
functions. It includes a review of the techniques by which
customers and suppliers can monitor one another via such
techniques as statistical analysis and auditing. The FDA
perspective, including the role and effect of FDA inspections,
is reviewed and particular attention is given to the problems
involved in contract work (i.e. outsourcing) with an emphasis
on the need for carefully defining the respective
responsibilities of the customer and supplier.<br><br>
The course includes a hands-on workshop in which miniteams
analyze case studies and present their findings.
11/17/2008
To
01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Medical Device
Course Category
Brochure Name
http://www.cfpa.com/PDF/2009/1984,C8-222,0902-404.pdf
Address
Amsterdam, The Netherlands Europe