This paper is in the following e-collection/theme issue:

Innovations and Technology in Cancer Research (35) Innovations in Clinical Trials and Research Data Management (84) Safety and Error Prevention in Health (206) Adverse Drug Events Detection, Pharmacovigilance and Surveillance (159) Cancer and Clinical Trials (20)

Published on in Vol 2, No 2 (2016): Jul-Dec

Clinical Trial Electronic Portals for Expedited Safety Reporting: Recommendations from the Clinical Trials Transformation Initiative Investigational New Drug Safety Advancement Project

Clinical Trial Electronic Portals for Expedited Safety Reporting: Recommendations from the Clinical Trials Transformation Initiative Investigational New Drug Safety Advancement Project

Clinical Trial Electronic Portals for Expedited Safety Reporting: Recommendations from the Clinical Trials Transformation Initiative Investigational New Drug Safety Advancement Project

Authors of this article:

Raymond P Perez1 Author Orcid Image ;   Shanda Finnigan2 Author Orcid Image ;   Krupa Patel3 Author Orcid Image ;   Shanell Whitney4 Author Orcid Image ;   Annemarie Forrest5 Author Orcid Image
Article Authors Cited by (6) Tweetations (1) Metrics

Raymond P Perez   1 , MD ;   Shanda Finnigan   2 , MPH, RN, CCRC ;   Krupa Patel   3 , BS ;   Shanell Whitney   4 , BS ;   Annemarie Forrest   5 , RN, MS, MPH

1 The University of Kansas Cancer Center, Kansas City, KS, United States

2 National Cancer Institute, National Institutes of Health, Bethesda, MD, United States

3 Merck Research Laboratories, Sudbury, MA, United States

4 Eli Lilly and Company, Indianapolis, IN, United States

5 Clinical Trials Transformation Initiative, Durham, NC, United States

Corresponding Author:

  • Annemarie Forrest, RN, MS, MPH
  • Clinical Trials Transformation Initiative
  • 300 W. Morgan St., Suite 800
  • Durham, NC
  • United States
  • Phone: 1 919 943 0358
  • Fax: 1 919 668 7039
  • Email: annemarie.forrest@duke.edu