Description
Government regulations have both explicit and implicit
requirements for an internal audit function in the
pharmaceutical and related industries. Auditing is a powerful
management tool in establishing how effectively a company
controls the quality of its products and ensures compliance.
The course will deal primarily with auditing techniques which
are applicable to any industry or function. Specific examples
will cover auditing of certain aspects of operations for
compliance with GMP, GCP and GLP. An FDA viewpoint on
auditing/inspecting will be presented. The course will consist
of lectures, discussions, exercises, workshops and a roleplaying
session involving a simulated compliance audit.<br><br>
The course is not designed for in-depth presentation of
regulatory issues, which are covered by other courses
offered by <b>CfPA.
01/01/0001
To
01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Clinical Research Organization
Course Category
Address
New Brunswick, NJ
New Brunswick,