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- W2153418614 abstract "Abstract A clinical trial site is an epicenter of clinical research, as the core action of clinical research happens here. Time and again sponsors and Clinical Research Organizations (CROs) have tried and used various parameters to assess a site. These parameters have been subjective, objective, and pragmatic. With effect from year 2013, Schedule Y has enhanced the role of Investigators and Institution's watchdog, i.e. Ethics Committee, which in turn has made a “site” more accountable. It is evident that the key stakeholders, e.g. sponsors, CROs, and regulators, are looking for objective data to support decisions like, which sites are the best and serve as long-term partners. After all, relationship between a drug manufacturer and a site/investigator, if turns out be a win–win, goes a long way. It is imperative that site identifies its core action points, monitor its performance and continuously improve. Through this article, the author has attempted to lay down some important top metrics (data points) site should focus on as part of their own continuous improvement initiatives." @default.
- W2153418614 created "2016-06-24" @default.
- W2153418614 creator A5008120713 @default.
- W2153418614 date "2015-10-01" @default.
- W2153418614 modified "2023-09-25" @default.
- W2153418614 title "Empowering clinical trial sites with data" @default.
- W2153418614 doi "https://doi.org/10.1016/j.injms.2015.09.002" @default.
- W2153418614 hasPublicationYear "2015" @default.
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