Topics addressed in this program will include:

•  A brief overview of the history behind ClinicalTrials.gov
•  Current statutory, regulatory and policy requirements for registering studies and reporting results information
•  A high level overview of how to create and maintain study records, including submission of results information

Click here to register for the session. Visit our website or join our mailing list for information on repeat sessions of this program. Submit advance questions or comments to ctgov@pitt.edu.

Speaker: Patrick Fawcett, ClinicalTrials.gov Coordinator