In this webinar, the panelists will describe the strategies used to develop and pilot the survey, administer the survey to HTC patients, and manage and analyze the data collected from respondents. Presenters will describe key national results and show how regional differences in participant demographics and diagnoses influence patient satisfaction.
When: September 22, 2016, 2 - 3 PM ET
What: Voices of 5,000+ Patients: The First National Survey on Experience of Care at U.S. Hemophilia Treatment Centers
Register here: http://bit.ly/28J750c