Factors Influencing Investigative Site Willingness and Ability to Participate in Clinical Trials

被引:0
|
作者
Mary Jo Lamberti
Rachael Zuckerman
Deborah Howe
Lisa Shapiro
Kenneth A. Getz
机构
[1] Tufts Center for the Study of Drug Development,Global Recruitment and Analytics
[2] Tufts University School of Medicine,Clinical Program Management
[3] Bristol-Myers Squibb,undefined
[4] Astellas Pharma Global Development. Inc,undefined
关键词
Investigative sites; Global clinical trials; Patient recruitment;
D O I
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中图分类号
学科分类号
摘要
The sponsor-site relationship is an essential consideration in investigative sites’ willingness to participate in clinical trials and sites’ ability to perform successfully. To better understand factors that impact this relationship, the Tufts Center for the Study of Drug Development, in conjunction with a working group of 10 pharmaceutical and biotechnology companies, developed a comprehensive two-part survey to examine clinical trial performance and investigator decisions to participate in a clinical study. Our respondents, clinical investigators worldwide, also provided company-specific ratings on training, investigator payments, receipt of supplies, study protocols, patient recruitment, and overall communication. A total of 3,516 surveys were completed for this study.
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页码:377 / 390
页数:13
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