Improved clinical trial methods including the use of subject monitors operating separately from standard clinical trial facilities and/or protocols. The subject monitors may independently or separately contact individual subjects to reinforce trial protocols, and observe compliance levels. Databases may be built and maintained for providing indications of the quality of a clinical trial. Clinical trial materials may be provided via the use of the independently operating subject monitors.
申请公布号
WO2007021727(A8)
申请公布日期
2007.04.12
申请号
WO2006US31013
申请日期
2006.08.09
申请人
CLINICAL SUPPLIES MANAGEMENT, INC.;FINKEN, GERALD, E.;SCHLECHT, KRISTINA, L.