Safety Monitoring(1.2CEU)

Class Number: 2066

Summer 2020

IT 9539

1.2 CEUs


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.




Course fee: $310

To access the online class, visit to log in after registration and payment using SF State ID and password.

Class Number: 2066


Refund Information

Refund Code Full Refund 75% Refund No Refund
CEL_1SUM Class dropped one day prior to class start day N/A Class dropped on or beyond class start day


Last Update: Jul 06, 2020 7:49pm