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University of Southern California
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Los Angeles, California
...
the reporting of Serious Adverse Events. Enters SAE into iStar for reporting to the IRB. Notifies Data ... Serious Adverse Events are experienced, follows FDA guidelines for prompt reporting within 24 hours
...
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University of Southern California
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Los Angeles, California
...
the reporting of Serious Adverse Events. Enters SAE into iStar for reporting to the IRB. Notifies Data ... Serious Adverse Events are experienced, follows FDA guidelines for prompt reporting within 24 hours
...
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University of Southern California
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Los Angeles, California
...
the reporting of Serious Adverse Events. Enters SAE into iStar for reporting to the IRB. Notifies Data ... Serious Adverse Events are experienced, follows FDA guidelines for prompt reporting within 24 hours
...