TITLE

Avoiding little mistakes-- and bigger problems

PUB. DATE
October 2010
SOURCE
Clinical Trials Administrator;Oct2010, Vol. 8 Issue 10, p115
SOURCE TYPE
Periodical
DOC. TYPE
Article
ABSTRACT
The article presents tips on preventing minor errors in clinical research documentation that could assist in solving major research problems. It stresses the importance of documenting the date with a stamp when the document is received from the institutional review board (IRB). Online sites are advised to avoid the use of notes to file to avoid questions that will arise in the future.
ACCESSION #
53917781

 

Related Articles

  • Compliance specialist finds these common informed consent errors.  // Clinical Trials Administrator;Aug2011, Vol. 9 Issue 8, p93 

    The article lists the informed consent errors found by a compliance specialist.

  • IC experts advocate improvements to process.  // IRB Advisor;Dec2011, Vol. 11 Issue 12, p126 

    No abstract available.

  • Videos help subjects, families understand trials.  // IRB Advisor;Jan2012, Vol. 12 Issue 1, p9 

    The article discusses a study by B. Hoffner and colleagues at Dana-Farber Cancer Institute in Boston, Massachusetts, which evaluated the impact of the clinical trials video on the knowledge of participants about the informed consent process. The study revealed no significant difference in...

  • Audits show researcher IC errors occur often.  // Clinical Trials Administrator;Aug2011, Vol. 9 Issue 8, p92 

    The article discusses the informed consent (IC) errors made by clinical trial sites with their prospective study participants and suggests ways to minimize them by developing a training series that focuses on IC for research staff. It suggests that they understand what auditors at research sites...

  • Expert tips on preventing persistent IC problems.  // IRB Advisor;Nov2011, Vol. 11 Issue 11, p118 

    The article presents questions and answers pertaining to the chief problems with the informed consent (IC) documentation and the ways in which those can be prevented.

  • Here are site source document sample IC items.  // Clinical Trials Administrator;Jul2011, Vol. 9 Issue 7, p79 

    The article offers information on source documentation checklists for site visits, screening visits, and other clinical research activities, created by UT Medical Group Inc. of Memphis, Tennessee. It explores a list of sample items included on the template for a screening visit, which includes...

  • The Informed Consent Process. Odeh, Peter // AMT Events;Mar2013, Vol. 30 Issue 1, p24 

    No abstract available.

  • Crucial steps to ensure good clinical practice.  // Clinical Trials Administrator;Oct2010, Vol. 8 Issue 10, p114 

    The article provides tips on acquiring an online site for a clinical trial that is efficient for tracking records in clinical practice. It notes the importance of having complete, exact and updated consent and documentation. Preparing source document worksheets is also suggested. The importance...

  • Response from the author. Vickers, Andrew J // Clinical Trials;Dec2014, Vol. 11 Issue 6, p628 

    No abstract available.

Share

Read the Article

Courtesy of VIRGINIA BEACH PUBLIC LIBRARY AND SYSTEM

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

Try another library?
Sign out of this library

Other Topics