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Previous validation tests conducted in 2008 proved that RIVA was effective in meeting requirements for compounding sterile doses (pre-publication data).
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For Niels Erik Hansen, Chief Executive Officer of IH Systems, the study results solidify the role of robotic automation in health care facilities. "The positive results of this study are very rewarding for the IH Systems team as the acceptance of advanced, robotic technology is dependant on its performance." These studies prove RIVA not only eliminates potential microbial contamination in the direct compounding area introduced by human contact but also reduces drug residue in the compounding environment and on surfaces of prepared doses. This overall reduction of drug residue lessens the adverse exposure of staff while processing hazardous drugs.
"The scrupulous research, development and commissioning program of the RIVA System has been integral in building confidence and support from directors of pharmacies worldwide," notes Jane Arnot, IH Systems VP Customer Sales and Service. "USP 797 and other regulatory guidelines set very strict parameters when it comes to sterility, accuracy and reduction of compounding risk, and meeting these requires a relentless commitment to excellence," she shares.
This study examined drug handling in the RIVA ISO 5 cell including the potential for drug cross contamination in final doses; drug contamination on surfaces in the cell; contamination on surfaces of final doses; and air contamination with drug both in the cell and in personal air samplers of workers who interact with the robot. Results demonstrated marked improvement over similar studies of hazardous drug handling.
RIVA (Robotic IV Automation System) - a self-contained unit for filling IV syringes and bags - is the first product developed by Winnipeg-based medical device company Intelligent Hospital Systems. For more information, please visit www.rivasystem.com.
SOURCE Intelligent Hospital Systems Ltd.