ClinicalTrials.gov
Thursday, January 30, 2014
1:00 pm - 3:30 pm
Sponsor(s): Duke Office of Clinical Research (DOCR)
ClinicalTrials.gov¿ Describe what ClinicalTrials.gov is and what it can do¿ Discuss why you should register your study (FDAAA & ICMJE)¿ Identify FDAAA required informed consent language¿ Identify who is responsible for registration (Responsible Party)¿ Discuss results reporting requirements¿ Describe how registration works at Duke¿ Identify Help Resources (institutional & national)¿ Discuss practice examples
Type: RESEARCH
Contact: DOCR
