MODERATOR
:
SPEAKER
(S):
Navneet Majhail, MD,MS, Medical Director, Health Services Research, National Marrow Donor Program
Roberta J. King, MPH, Vice President, CIBMTR Minneapolis, National Marrow Donor Program
Description
Blood and stem cell donors are increasingly being requested to participate in research protocols involving their donation or as third parties to patient focused research. On the basis of current regulations and ethical principles of human subject protections, the faculty will discuss how to determine if a donor is a research subject or a third party in research. In addition, this session will also discuss how to approach donors about research studies and provide case examples of how to share information with donors.
LEARNER OUTCOMES:
-
Describe key elements of informed consent for donors.
-
Determine how to approach donors about research and explain studies appropriately so the donor is prepared to make an informed decision about whether or not to participate.
-
Evaluate a method for determining whether or not a donor is considered a research subject or a third party in patient focused research.
| CE Category | CE Value |
|---|
|
California Clinical Laboratory Personnel |
1.5 |
|
California Nurse |
1.8 |
|
Florida Laboratory Personnel |
1.8 |
|
General Attendee |
1.5 |
|
Physician |
1.5 |
Please note: Continuing education (CE) credit is available for online offerings only. Individuals that purchase CD-ROMs will not receive CE credit for the programs they view.