Send us your interest if this course is currently not offered or the current schedule does not accomodate your schedule. It is often necessary to understand interest a semester in advance for planning and scheduling. Companies and organizations can often request a course if the group is large enough. This doesn't mean that we can make accommodations in every case. However, we will utilize and maximize our available resources as best as we can. Thanks for letting us know your interests and we will respond as soon as we can.
Learn the use of a master validation plan, Installation Qualification (IQ), Operational qualification (OQ), and Performance Qualification (PQ) protocols, and the relationship of validation to Good Manufacturing Practices (GMPs). Through case studies and exercises, participants learn the fundamental requirements of preparing a validation protocol, analyzing data, and preparing a final report. FDA inspection expectations are also discussed.
Each college has their own registration process.
We make every attempt to make it seamless.