Human Subjects Research at Duke Overview
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Thursday, July 10, 2014
9:00 am - 11:00 am
Donna Hamel
Study Documentation Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Thursday, August 14, 2014
9:00 am - 11:00 am
Catee Mullen
Human Subjects Research at Duke Overview
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Thursday, August 21, 2014
9:00 am - 11:00 am
Phyllis Kennel
Human Subjects Research at Duke Overview
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Thursday, October 09, 2014
9:00 am - 11:00 am
Phyllis Kennel
Research Database Design
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Wednesday, December 03, 2014
2:00 pm - 4:00 pm
Sue Budinger, Jeff Hawley, Ceci Chamorro
Human Subjects Research at Duke
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Wednesday, April 29, 2015
9:30 am - 11:30 am
Study Documentation Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Wednesday, April 29, 2015
11:30 am - 1:30 pm
The Informed Consent Process
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Wednesday, May 06, 2015
10:00 am - 12:00 pm
Adverse Events
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, June 09, 2015
2:00 pm - 4:00 pm
Population Segmentation Based on Needs: What, Why, and How?
Sponsor(s):
Population Health Sciences
Wednesday, February 07, 2018
12:00 pm - 1:00 pm
Dr. David Matchar, MD