Presentation
Presented on: July 12, 2016
Presented at: Third Clinical Regulatory Medical Writing Forum, Philadelphia, PA
Focus Area: Clinical Trials & Research
Fourth Clinical Regulatory Medical Writing Forum
Presentation
Presented on: July 10, 2017
Presented at: 4th Clinical Regulatory Medical Writing Forum in Philadelphia
The Voice of the Patient – Returning Aggregate Results through Plain Language Summaries
Presentation
Presented on: June 23, 2019
Presented at: DIA 2019 Global Annual Meeting in San Diego
Current and Ongoing Data Transparency Activities in the Pharmaceutical Industry
Public Comments
Comments provided on: October 1, 2014
Comments provided to: Standing Senate Committee on Social Affairs, Science and Technology, Canada
Submission of comments on Draft proposal for an addendum, on transparency, to the ‘Functional specifications for the EU portal and EU database to be audited’
Public Comments
Comments provided on: February 18, 2015
Comments provided to: European Medicines Agency, United Kingdom
Compliance with Results Reporting at Clinical Trials.gov
Publication
Published on: June 11, 2015
Published in: The New England Journal of Medicine
“Proposed Rule – Clinical Trial Registration and Results Submission” Comments to NIH
Public Comments
Comments provided on: March 20, 2015
Comments provided to: National Institutes of Health
Harvard MRCT Annual Meeting 2014
Proceedings
Proceedings from: Harvard MRCT 2014 Annual Meeting on December 3, 2014
Held at: Loeb House, Harvard University
Health Research Authority – Guidance on participant information at the end of a study
Public Comments
Comments provided on: October 3, 2014
Comments provided to: Health Research Authority, UK
Summary of Clinical Trial Results for Laypersons – Comments to European Medicines Agency
Public Comments
Comments provided on: August 16, 2016
Comments provided to: European Medicines Agency, UK