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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?
Where Should Electronic Records for Patients be Stored?
To help identify the architecture best suited for efficient and complete nationwide health information exchange based on the large-scale operational characteristics of these architectures.
MAQUET Takes Over U.S. Distribution of Jostra Product Line
Dear Customer: Effective April 5, 2004 NOVOSCI will cease to be the distributor of Jostraproducts in the United States and MAQUET Inc. […]