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Notice of Changes to Prior Authorization/Registration Requirements
To provide information on CareCentrix's prior authorization/registration requirements and changes to those requirements...
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FDA Recall - Baxter International, Inc.
We are writing to inform you that effective immediately the FDA has issued notice of a voluntary urgent recall of the Life2000 ventilator with an attached battery charger dongle...
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Changes to Provider Demographic Information
To remind providers that they must timely notify CareCentrix of any changes in their demographic information or changes to the information submitted in their CareCentrix credentialing application...
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