The Clinical Trials Registration and Results Reporting Taskforce is a national consortium of members of academic medical centers, universities, hospitals, and non-profit organizations focused on the implementation of domestic clinical trials registration and results reporting requirements in the ClinicalTrials.gov public repository. The objectives of the group are to identify best practices, develop solutions and tools for regulatory support and investigators, and serve as a communication forum.

 

Do you have a topic that you would like to discuss at an upcoming taskforce meeting? Please email Sarah or Tony.

Taskforce Sightings!

Members of the Taskforce met at the PRIM&R Advancing Ethics in Research Conference in Boston, November 19, 2019. 

ctgovprimr

Pictured from left to right is Dawn Lundin (University of Pennsylvania), Katherine Bode-Lang (Pennsylvania State University), Amelia Walch-Patterson (Ochsner Health System), Sarah White (MRCT), Anthony Keyes (Johns Hopkins), Debra Stavarski (Tower Health), Shakira Forde (Einstein), Sarah Snider (Medical University of South Carolina), Melanie Chladny (University of Michigan), Jennifer Farmer (Virginia Tech), Carley Emerson (Carillion Clinic).

On September 20, 2019 Taskforce members met up for lunch and robust discussion at the DIA Global Clinical Trial Disclosure and Data Transparency Conference in Washington, DC.

TaskforceatDIA

Pictured [left to right]: Anthony Keyes (Johns Hopkins), Kelly Mulvaney (Kansas), Rhonda May (Kansas), Patrick Fawcett (Pittsburg), Rebecca Chen (Rutgers), Diane Lehman Wilson (Michigan), Erin McDonagh (University of Colorado Denver) and Johns C. Hicks (Oregon Health & Science University)