Advanced Track (SBER)

2019 SBER Conference

Advanced

C04 - Clinical Trials in SBER (ClinicalTrials.gov Registration)—Part II

Speaker(s)

• 

  Kate Sasamoto, JD
  

  Senior Research Compliance Associate, Office of Research Compliance Review, University of Michigan
  
• 

  Wendy J. Weber, ND, PhD, MPH
  

  Clinical Research Branch Chief, Division of Extramural Research, National Center for Complementary and Integrative Health
  

NIH-funded research projects meeting the NIH definition of clinical trials must be registered and results reported on ClinicalTrials.gov. For investigators and institutions that do not typically work with clinical trials, meeting these requirements can be challenging. This session is designed to provide an overview and tips for assisting SBE researchers and institutions with ClinicalTrials.gov responsibilities. Before attending this session, attendees should be familiar with the content presented in A2: Clinical Trials in SBER (NIH and OHRP Overview), or have basic knowledge of ClinicalTrials.gov. During this session, speakers and attendees will:

Learning Objectives:

• Review requirements for registering a study on ClinicalTrials.gov
• Discuss continuing obligations regarding active ClinicalTrials.gov records
• Describe the process for reporting study results on ClinicalTrials.gov
• Note: Part I of this session will take place from 9:15-10:30 AM (Session A2).