Subject: Is your organization ready to respond to the *next* paclitaxel?

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In other words - what processes do you have in place to incorporate new information quickly into clinical practice—especially when there's uncertainty around patient safety?

We're still thinking about OhioHealth system's quick response to the paclitaxel controversy last year, which we touched on in our last Quality Matters news brief—and we want to hear your perspective. 

Does your organization have robust processes in place to respond quickly to new clinical information?
Don't have a Twitter? Send me a quick reply - 
I'd love to add your perspective to the conversation.

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Kurt Jensen
Communications Director
Association/Foundation Headquarters, PO Box 2007, 23113, Midlothian, United States
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