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Expand your knowledge in the application of current good manufacturing practices (cGMP) in the production of biopharmaceuticals. An overview of topics will be covered from current regulations found in the selections of 210/211 of Title 21 of the Code of Federal Regulations (CFR) as well as the relevant ICH and FDA guidance documents.
Lab Hours: 0.00
Lecture Hours: 16.00
Total Contact Hours: 16.00