Get the free Produced by ECRI & ISMP under contract to the Pennsylvania Patient Safety Authority
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Patient Safety AdvisoryReprinted from the PAPERS Patient Safety Advisory. 2, No. 3 (Sept. 2005)Produced by ECRU & ISP under contract to the Pennsylvania Patient Safety AuthorityProblems Associated
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What is produced by ecri amp?
The ECRI AMP produces reports on medical device safety issues.
Who is required to file produced by ecri amp?
Manufacturers, distributors, and importers of medical devices are required to file reports produced by ECRI AMP.
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The reports produced by ECRI AMP can be filled out online through their reporting system.
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The purpose of reports produced by ECRI AMP is to track and monitor safety issues related to medical devices.
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The reports produced by ECRI AMP must include information on adverse events, malfunctions, and other safety issues related to medical devices.
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