Description
<strong>Course Schedule - 11-13 March 2009</strong><br/><br/>This course provides a detailed description of the
current European and US regulations for medical
devices. With the continued growth in the development
and acceptance of global standards, all device
companies must stay up to date on the various
regulations to ensure marketability of their products
globally. With 27 European countries now using the
ISO 13485 standard, it is critical to companies to
understand how the similarities and differences in
these standards can be implemented into their
own quality system to enhance their marketability.
The primary focus of this course is on the development
of one quality system which complies with the ISO
13485:2003 standard, ISO 9001:2000 standard and
the FDA Quality System Regulations.<br><br>
Participant interaction, problem solving and open
discussion will be strongly encouraged.
11/14/2008
To
01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Pharmaceutical
Course Category
Brochure Name
http://www.cfpa.com/PDF/2009/2092,C8-251,0903-406.pdf
Address
Dublin, Ireland Europe