Streamlining Adverse Events Reporting in Oncology: An American Society of Clinical Oncology Research Statement-Reference-Cited by-同舟云学术

Streamlining Adverse Events Reporting in Oncology: An American Society of Clinical Oncology Research Statement

Published:2018-02-20 Issue:6 Volume:36 Page:617-623
ISSN:0732-183X
Container-title:Journal of Clinical Oncology
language:en
Short-container-title:JCO

Author:

Levit Laura A.¹,Perez Raymond P.¹,Smith David C.¹,Schilsky Richard L.¹,Hayes Daniel F.¹,Vose Julie M.¹

Affiliation:

1. Laura A. Levit and Richard L. Schilsky, American Society of Clinical Oncology, Alexandria, VA; Raymond P. Perez, Bristol-Myers Squibb, Lawrence Township, NJ; David C. Smith and Daniel F. Hayes, University of Michigan, Ann Arbor, MI; and Julie M. Vose, University of Nebraska Medical Center, Omaha, NE.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

Link

https://ascopubs.org/doi/pdfdirect/10.1200/JCO.2017.75.8193

Reference24 articles.

1. Sponsors’ and investigative staffs' perceptions of the current investigational new drug safety reporting process in oncology trials

2. The Majority of Expedited Investigational New Drug Safety Reports Are Uninformative

3. Addressing Administrative and Regulatory Burden in Cancer Clinical Trials: Summary of a Stakeholder Survey and Workshop Hosted by the American Society of Clinical Oncology and the Association of American Cancer Institutes

4. New FDA Regulation to Improve Safety Reporting in Clinical Trials

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