Process Validation for Biopharmaceutical Manufacturing

Process Validation for Biopharmaceutical Manufacturing

This course reviews the regulatory requirements and methods for validating pharmaceutical and biopharmaceutical manufacturing processes. Topics covered, include: The history of Process Validation; Risk based analysis; QbD (Quality by Design); PAT (Process Analytical Technology); DOE (Design of Experiments); Process optimization and characterization.

Currently, there are no upcoming courses.

Interest Form

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.

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