More efficient systems improve site compliance

April 2007
Clinical Trials Administrator;Apr2007, Vol. 5 Issue 4, p42
The article discusses how medical research site compliance could be enhanced. Kris Rhodes of Wake Forest University Health Sciences in Winston-Salem, North Carolina stressed the importance of recording the contract negotiating positions in policies of research sites. She stressed that staff should be informed and trained of their positions. She suggested using billing system, checking effort reporting and depending on systems to operate reports in sponsored research.


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