Description
This course will provide a <b>basic</b> understanding of the
technology transfer of analytical methods, quality control
standards, packaging components/operations and various
pharmaceutical dosage forms from R&D to manufacturing. It
is designed to provide an understanding of the issues
affecting the transfer within and outside a company. Topics
will include transfer of technology to/from international sites
as well as to/from third parties. Regulatory requirements and
recommended approaches will be discussed. Speakers will
use practical examples to highlight issues critical to
successful technology transfer. Best practices from several
pharmaceutical companies and contract manufacturers will be
presented and contrasted.