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Guidance To Improve Safety And Mitigate Risk
The FDA is taking action over concerns that medical devices, which exchange data and information on a patients health, are made to function safely, accurately, and securely. With the recent release of new draft guidance, the FDA is hoping to address issues with healthcare industry cybersecurity, device interoperability, and additional risks that are present when technicians, system integrators, and other third parties must be involved in making devices and systems operable. The agency is also seeking to help manufacturers avoid errors and inconsistencies that could result in inaccurate measurements, disfunction, mislabeling and misinformation that might result in patient harm or even death.

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Catching Up With The Technology We Create
With the pace of technology and the potential it has for saving and bettering lives, it appears that we still have some catching up to do when it comes to safe and reliable integration of advanced medical devices. Will the new FDA guidance help make things easier for manufacturers and improve safety and security for patients and health care providers? Tell us what you think in the comments.
Article Sources:
http://www.modernhealthcare.com
http://www.fda.gov
http://www.reuters.com
Why Connectivity Is A Major Concern In Medical Manufacturing And Healthcare was first published to Magoda | Manufacturing America by ROIGROUP
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