Description
<strong>Course Schedule - May 18-20, 2009</strong><br/><br/>This course will present information on microbiological control
in manufacturing, laboratory auditing and sterilization. The
course will also cover ISO, EP, BP, USP, AAMI and U.S. FDA
documents and guidelines. Validation of sterilization processing
will be discussed and case studies will be presented.
Environmental monitoring programs will be discussed in depth.
Design and testing of product packages for sterility assurance
will be covered via case studies. All aspects of microbiological
control will be covered. Microbiological testing schemes will be
presented and the key aspects of GLP/cGMP will be
reviewed. You are invited to bring transparencies of monitoring
programs, procedures, flowcharts, etc., for discussions during
the case studies on the third day.
