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In light of the existing concerns on HES use, this study leaves several unanswered questions: how should patients be informed when they are asked to participate in a clinical trial that may randomise them to receive HES? How can a prestigious research group consider it appropriate to adopt a ’non‐inferiority’ study design to evaluate the safety profile of a controversial drug such as HES, when any proven beneficial effects (if there are any) remain unanswered?
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The Pennsylvania Legislature Today Passed House Bills 500 and 501 Enacting Licensure of Perfusionists in Pennsylvania
The Pennsylvania Legislature today passed House Bills 500 and 501 enacting licensure of perfusionists in Pennsylvania.
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World Heart Gains FDA Approval for Novacor Changes
World Heart Corp. said on Wednesday it obtained pre-market approval from the U.S. Food and Drug Administration (FDA) for engineering changes to […]
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