TITLE

Have We Pushed Our Pis Too Far?

AUTHOR(S)
Getz, Kenneth A.
PUB. DATE
September 2005
SOURCE
Applied Clinical Trials;Sep2005, Vol. 14 Issue 9, p34
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Looks at what clinical trial sponsors and clinical research organizations can do to ease the performance, compliance, and financial pressures faced by clinical investigators. Growing signs that the base of clinical investigators in the United States is weakening; Major threats that the tenuous and changing principal investigator landscape poses to research sponsors and research organizations; Concerns raised by investigators regarding the size of grant amounts and the slow payment process.
ACCESSION #
18196870

 

Related Articles

  • WHO seeks system for tracking global clinical trials. Check, Erika // Nature;11/11/2004, Vol. 432 Issue 7014, p137 

    The article presents a report on a system for tracking global clinical trials. The World Health Organization (WHO) hopes to earn international support next week for a far-reaching plan to set up a global tracking system for clinical trials. These measures are intended to reduce the duplication...

  • Doctors are not scientists. Smith, Richard // BMJ: British Medical Journal (International Edition);6/19/2004, Vol. 328 Issue 7454, p0 

    Offers a look at the benefit of supplying scientific studies to physicians. Statement that physicians are not scientists; Inability of most physicians to read scientific medical research and aptly analyze its merits; Importance of peer reviewers; Reference to an article in the June 19, 2004...

  • Communicating the Results of Clinical Research to Participants: Attitudes, Practices, and Future Directions. Shalowitz, David I.; Miller, Franklin G. // PLoS Medicine;May2008, Vol. 5 Issue 5, pe91 

    The authors discuss the available data on the effects of communicating aggregate and individual research results on participants, investigators, and the research enterprise.

  • Origin and funding of the most frequently cited papers in medicine: database analysis. Patsopoulos, Nikolaos A.; Ionnidis, John P. A.; Analatos, Apostolos A. // BMJ: British Medical Journal (International Edition);5/6/2006, Vol. 332 Issue 7549, p1061 

    Objective To evaluate changes in the role of academics and the sources of funding for the medical research cited most frequently over the past decade. Design Database analysis. Data sources Web of Knowledge database. Methods For each year from 1994 to 2003, articles in the domain of clinical...

  • Measuring Investigator Satisfaction. McClelland, Graham; Siegel, Judith L.; Goddard, Melinda K.M. // Applied Clinical Trials;Jun2002, Vol. 11 Issue 6, p70 

    Focuses on the identification of Roche trials for measuring investigator satisfaction. Relationship between clinical investigators and pharmaceutical companies; Ways to improve customer through investigator satisfaction; Limitation of opportunities to conduct trials.

  • Conducting Clinical Trials in ASIA. Varawalla, Nermeen // Applied Clinical Trials;Sep2010 Retrospective Supplement, p8 

    The article focuses on clinical trials in Asia. It states that sponsors are interested to perform clinical trials in the region because of rapid patient recruitment, savings in costs, world-class investigational sites and well-trained clinical investigators. It also states that data on clinical...

  • Clinical Trials in India. Bobba, Radhika; Khan, Yamin // Applied Clinical Trials;Feb2003, Vol. 12 Issue 2, p52 

    Focuses on the ethical implications of conducting clinical trials in India. Factors affecting the decision of clinical investigators in conducting clinical trials in exotic locations; Total number of government and privately owned hospitals engaged in clinical trials; Comparison between...

  • The Pulse on Study Conduct. Weeks-Rowe, Elizabeth // CenterWatch Weekly;11/7/2016, Vol. 20 Issue 44, p6 

    The article discusses the requirements of the clinical research study and gives information on the role of clinical investigator, regulatory agency, and events that can occur during the study.

  • The Invisible Hand in Clinical Research: The Study Coordinator's Critical Role in Human Subjects Protection. Davis, Arlene M.; Hull, Sara Chandros; Grady, Christine; Wilfond, Benjamin S.; Henderson, Gail E. // Journal of Law, Medicine & Ethics;Fall2002, Vol. 30 Issue 3, p411 

    Focuses on the critical role of study coordinators in clinical research. Growth of the business of clinical research in the community settings; Roles of caregiver and researcher on clinical investigation; Impact of the study coordinator on the protection of human subjects.

Share

Read the Article

Courtesy of THE LIBRARY OF VIRGINIA

Sorry, but this item is not currently available from your library.

Try another library?
Sign out of this library

Other Topics