$310
Collection, monitoring and evaluation of safety data is a key responsibility of the Sponsor and Investigator and the first goal listed by the FDA. Adverse events and serious adverse events are key data elements to review the safety of a product. An adverse event is defined as an untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product that does not necessarily have a causal relationship with this treatment. This course will introduce you to common safety monitoring practices and the regulatory reporting responsibilities for medical products.
Dates | Days and Times | Location | Faculty |
---|---|---|---|
4/20/21-5/25/21 | Tues, 6:00PM-7:30PM | Online | Bethany Van Veen |
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Course fee: $310
To access the online class, visit http://ilearn.sfsu.edu to log in after registration and payment using SF State ID and password.
Refund Code | Full Refund | 75% Refund | No Refund |
---|---|---|---|
CEL_1 | Class dropped one day prior to class start day | N/A | Class dropped on or beyond class start day |
Last Update: Mar 03, 2021 5:03pm