Study start-up site communication plan

March 2011
Clinical Trials Administrator;Mar2011, Vol. 9 Issue 3, p31
The article presents an overview of the site start-up team communication plan developed by the Duke Clinical Research Institute (DCRI), Durham, North Carolina, and highlights the plan's aspects including site regulatory contact, site legal document contact and legal documents.


Related Articles

  • Managing Quality in Clinical Research. Besnard, Susan // Applied Clinical Trials;Apr2000, Vol. 9 Issue 4, p65 

    Discusses various concepts related to achieving quality in clinical trials. Definition of the term `quality assurance' in the context of clinical research; Concepts and terms pertaining to good clinical practice (GCP); Applicability of standards created by the International Organization for...

  • Techniques and Strategies for Improvement. Legg, Jeffrey S. // Radiologic Science & Education;Jul2012, Vol. 17 Issue 1, p1 

    An introduction to the journal is presented in which the editor discusses several article within the issue on topics including, Problem-Based Learning (PBL) in radiologic science education, a research analyzing student's success and tailoring clinical education to the individual student's needs.

  • Three Steps to Better Decisions. Connor, Kevin // Applied Clinical Trials;Feb2013, Vol. 22 Issue 2, p42 

    The article presents information on the clinical trial-based decisions which allows pharmaceutical companies to decide whether to launch a product or terminate its development. It mentions about collaborative prioritization in which decision makers including scientists, physicians, and quality...

  • External Quality Assurance Performance of Clinical Research Laboratories in Sub-Saharan Africa. Amukele, Timothy K.; Michael, Kurt; Hanes, Mary; Miller, Robert E.; Jackson, J. Brooks // American Journal of Clinical Pathology;Nov2012, Vol. 138 Issue 5, p720 

    Patient Safety Monitoring in International Laboratories (JHU-SMILE) is a resource at Johns Hopkins University that supports and monitors laboratories in National Institutes of Health-funded international clinical trials. To determine the impact of the JHU-SMILE quality assurance scheme in...

  • Better Reporting of Harms in Randomized Trials: An Extension of the CONSORT Statement. Ioannidis, John P.A.; Evans, Stephen J. W.; G√łtzsche, Peter C.; O'Neill, Robert T.; Altman, Douglas G.; Schulz, Kenneth; Moher, David // Annals of Internal Medicine;11/16/2004, Vol. 141 Issue 10, p781 

    In response to overwhelming evidence and the consequences of poor-quality reporting of randomized, controlled trials (RCTs), many medical journals and editorial groups have now endorsed the CONSORT (Consolidated Standards of Reporting Trials) statement, a 22-item checklist and flow diagram....

  • Quality assurance of drugs used in clinical trials. Newton, Paul N.; Schellenberg, David; Ashley, Elizabeth A.; Ravinetto, Raffaella; Green, Michael D.; ter Kuile, Feiko O.; Tabernero, Patricia; White, Nicholas J.; Guerin, Philippe J. // BMJ: British Medical Journal;2/28/2015, Vol. 350 Issue 7997, ph602 

    The article reports that clinical trial guidelines from international organizations like the World Health Organization (WHO) should be updated to include a requirement for assessing the quality of drugs and medical products used in clinical research. Topics covered include clinical trials...

  • Quality assurance of radiotherapy in the ongoing EORTC 22042-26042 trial for atypical and malignant meningioma: results from the dummy runs and prospective individual case Reviews. Coskun, Mehtap; Straube, William; Hurkmans, Coen W.; Melidis, Christos; de Haan, Patricia F; Vill√†, Salvador; Collette, Sandra; Weber, Damien C. // Radiation Oncology;2013, Vol. 8 Issue 1, p1 

    Background: The ongoing EORTC 22042-26042 trial evaluates the efficacy of high-dose radiotherapy (RT) in atypical/malignant meningioma. The results of the Dummy Run (DR) and prospective Individual Case Review (ICR) were analyzed in this Quality Assurance (QA) study. Material/methods:...

  • Here are some steps to follow in negotiations.  // Clinical Trials Administrator;Feb2011, Vol. 9 Issue 2, p22 

    No abstract available.

  • Easing the paper-to-EHR transition. Mullen, Kevin // Health Management Technology;Apr2012, Vol. 33 Issue 4, p18 

    The article discusses a project on transitioning from paper to electronic health records (EHRs). It makes reference to the Beth Israel Deaconess Medical Center (BIDMC) and Beth Israel Deaconess Physician Organization (BIDPO) project that will provide EHRs to affiliated physicians across eastern...


Read the Article


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

Try another library?
Sign out of this library

Other Topics