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    Monthly Archive for: "September, 2017"
    Home » Archives for September 2017
     How do patient preferences influence medical device regulations?
    By Chris Ross
    In Medical Product Design
    Posted September 29, 2017

    How do patient preferences influence medical device regulations?

    For organizations involved in medical device design and development, it’s important to be aware of the ramifications that patient preference could have on the path to regulatory clearance.

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     How to Break the Curse of Habit
    By Chris Ross
    In Human Factors & Usability Testing, Medical Product Design
    Posted September 29, 2017

    How to Break the Curse of Habit

    Our brains are like a GPS mapping app, automatically adapting to a constant stream of information and only occasionally asking us to choose an alternative route. That automatic decision-making [...]

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     How new regulations are changing the market for medical devices in Europe
    By Chris Ross
    In Medical Product Design
    Posted September 27, 2017

    How new regulations are changing the market for medical devices in Europe

    By understanding the effects of MDR and IVDR and strategizing accordingly, makers of medical products can position themselves to meet the challenges of competing in the European market.

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     What can medical device firms learn from a pacemaker recall?
    By Chris Ross
    In Medical Product Design
    Posted September 19, 2017

    What can medical device firms learn from a pacemaker recall?

    By prioritizing cybersecurity, makers of medical products are strategizing for the future of healthcare.

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      These Are the Contents of a Proper Product Requirements Document
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      Your Medical Device’s User Interface Specification Is More Powerful Than You Think
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    • Risk Management Simplified: Streamline Your FDA Submission with a Hazard Analysis Worksheet
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      Does Your Medical Device Need Design Controls? Here’s What You Need to Know.
      June 20, 2023
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