Description
This course prepares attendees to meet the challenges
they face in this heavily regulated industry. It is vital for API
producers to ensure that GMP principles are applied to API
production and control, and to demonstrate knowledge of
FDA, ICH and other governmental and industry guidance
documents.<br><br>
This course will provide guidance in the design, construction,
and validation of GMP pilot and production facilities. Examples
of facilities will be discussed. The selection, qualification, and
cleaning of equipment will be included with specific examples.
Process validation is of singular importance and validation
principles and their application will be demonstrated with
examples. Process development and technical transfer
reports will be described. The function of the quality unit
to establish and manage the systems required to maintain
compliance will be discussed. Throughout the program there
will be interactive class exercises. On the last day of the
course participants will receive instruction on managing an
FDA inspection followed by a workshop in which participants
prepare written responses to simulated FD-483s (List of
Inspectional Observations) based on actual FDA
observations. The exercise will result in a valuable exchange
of information and approaches with your colleagues.
01/01/0001
To
01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Pharmaceutical
Course Category
Address
New Brunswick, NJ
New Brunswick,