|
(back)
|
|
|
This presentation will review the new Informed Consent Form templates developed by the Health Sciences IRB Office, as well as common errors that can be prevented when writing an informed consent document.
|
Emily Putman-Buehler (emily.putman@wisc.edu)
|
Tina Graber, Regulatory Specialist, Office of Clinical Trials
Jennifer Fenne, Senior IRB Analyst, HS IRB
|
|
|
|
Official Course Website
|
|
|
|
No upcoming events.
|