Create tools to facilitate efficient documentation

July 2011
Clinical Trials Administrator;Jul2011, Vol. 9 Issue 7, p77
The article discusses that clinical research sites should create their own coordinator tools and source documents to include information needed for compliance with research regulations in order to improve documentation efficiency. It offers information on the checklists and templates used at UT Medical Group Inc. of Memphis, Tennessee. Included are comments from the company's manager of clinical trials operations, Derita Bran.


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