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AAMI TIR57: 2016

Principles for medical device security - Risk management

Provides guidance on methods to perform information security risk management for a medical device in the context of the Safety Risk Management process required by ISO 14971. The TIR incorporates the expanded view of risk management from IEC 80001-1 by incorporating the same key properties of Safety, Effectiveness and Data & Systems Security with Annexes that provide process details and illustrative examples.


Content Provider
Association for the Advancement of Medical Instrumentation [aami]


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Principles for medical device security - Postmarket risk management for device manufacturers
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Medical device software - Part 1:Guidance on the application of ISO14971 to medical device software
Document History
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As the voice of the U.S. standards and conformity assessment system, the American National Standards Institute (ANSI) empowers its members and constituents to strengthen the U.S. marketplace position in the global economy while helping to assure the safety and health of consumers and the protection of the environment.

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