ClinicalTrials.gov: Background, Requirements & Process

August 23, 2017 -
11:30am to 12:30pm

Speaker: Patrick Fawcett, ClinicalTrials.gov Coordinator

Topics addressed in this session 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 program as seating is limited.  The session will be repeated on September 20, 2017.
Submit advance questions or comments to ctgov@pitt.edu.

Location and Address

RCCO Learning Resource Center, Room 305
Hieber Building, 3500 Fifth Avenue