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Thursday, April 23 • 11:00am - 12:00pm
What the CTN Needs to Know About Submitting Results to ClinicalTrials.gov (Clinical Trial Nurses SIG)

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Since the Food and Drug Administration Amendments Act of 2007, the scope of clinical trials required to be registered and the requirements of reporting results on ClinicalTrials.gov have expanded. The clinical trials nurse (CTN) may be directly involved with any part of this process. In this session, you’ll explore the rationale for the registry and how data are reported to comply with the law and better answer patient questions related to information found on the website.


  1. Discuss the scientific and ethical rationale behind registering clinical trials and reporting results.
  2. Define which trials are required to be registered and have results submitted to ClinicalTrials.gov.
  3. Discuss the process for submitting results to ClinicalTrials.gov.
  4. Identify resources to assist with registration and results submissions.

avatar for Rebecca Williams

Rebecca Williams

Assistant Director, ClinicalTrials.gov, NCBI, National Library of Medicine, NIH
As the Assistant Director of ClinicalTrials.gov, Dr.Williams is responsible for the results submission process, outreach and education, policy and regulation development, and research related to evaluating and improving reporting of clinical research.

Thursday April 23, 2015 11:00am - 12:00pm
414CD 9800 International Drive, Orlando, FL 32819