With the Exit Dose module, Dosimetry Check allows for both pretreatment quality assurance and in vivo dose verification. In vivo dose allows a clinician to see the dose delivered to a patient, so treatments can be assessed and modified in the remaining fractions, if necessary.
The Exit Dose option has recently received 510(k) clearance from the U.S. Food and Drug Administration, and it previously received the European CE Mark.
CIVCO launches new guidance systems, August 6, 2010
CIVCO completes 2 installs, July 19, 2010
CIVCO adds to portfolio, June 22, 2010
CIVCO introduces new fiducial markers, June 4, 2010
CIVCO launches needle guidance system, March 1, 2010
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