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Clinical Trial Resources


Conducting clinical investigation in oncology is an integral part of the professional activities of oncologists and serves the mission of improving the survival and quality of life for cancer patients. With this statement, ASCO Statement on Minimum Standards & Attributes of Exemplary Clinical Trial Sites, ASCO affirms the basic standards for conducting research (compliance with Good Clinical Practice (GCP) guidelines), as well as describes the characteristics of exemplary sites.

An ongoing article series in the Journal of Oncology Practice will provide practical information on how to implement the GCP guidelines and exemplary attributes. Topics will include: implementing GCP, promoting quality assurance, continuing education, working with your IRB(s), developing a cost neutral clinical research enterprise, surviving the audit process, marketing and outreach, and enhancing your participation in the research process.

ASCO Outlines minimum Standards & Exemplary Attributes for Research Sites: Preview tools to Be Provided (JOP Jul 2008: 185-187.)

Good Clinical Practice Research Guidelines Reviewed, Emphasis Given to Responsibilities of Investigators: Second Article in a Series (JOP Sep 2008: 233-235.)

Quality Assurance and Educational Standards for Clinical Trial Sites (JOP Nov 2008: 280-282)

Exemplary Attributes: How to Prepare for an Audit (JOP Jan 2009: 35-37)

Cost-Neutral Clinical Research Enterprise (JOP March 2009: 76-79)

Enhancing Clinical Trials Awareness and Outreach (JOP July 2009: 205-207)

Working With Your Institutional Review Board (JOP Sept 2009: 256-258)

The next article in this series will discuss how to enhance your participation in research, including information on making the most out of attending Cooperative Group meetings and building relationship with private research networks .

Email researchresources@asco.org to be notified as new articles, tools and resources become available.





 
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