Description
<strong>Course Schedule - June 1-3, 2009</strong><br/><br/>This course will prepare you to meet the varied challenges
now facing the global active pharmaceutical ingredient
industry. It is important that API production facilities operating
under different national and international regulatory authorities
not be required to meet diverse standards. For this reason an
Expert Working Group in ICH developed the ICH-Q7
document as a single standard that all suppliers must apply to
production of APIs used in human drug products
manufactured in any of the ICH signatory regions.<br><br>
This course will provide historical insight into the development
of the Q7 document and specific interpretation of
requirements in the document. The Q7 document addresses
all aspects of API production in 19 sections. Each of these
sections will be examined in detail during the course.
Throughout the formal presentations participation by the
registrants is welcome.<br><br>
There are interactive exercises periodically spaced through
the first two days that allow registrants to analyze real life
situations that occur in typical operations. These afford an
opportunity to exchange information and approaches with
colleagues. The final activity is a workshop in which
registrants are asked to apply what they have learned to
resolve issues in test cases.
01/13/2009
To
01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Biotech
Course Category
Brochure Name
http://www.cfpa.com/PDF/2009/2091,C8-219,0906-101.pdf
Address
New Brunswick, NJ USA