Health Canada published a notice entitled “Software Regulated as a Class I or Class II Medical device,” along with a Q&A memo to clarify what software is regulated and which regulations apply. Both documents are included at the link provided. The notice appears to indicate that any software which fits the definition of a medical...Read More
The AAMI Human Factors committee has proposed a work item to develop a new standard: “AAMI/HE N245R2, Human factors engineering design processes for medical device software not considered a medical device”.The current proposal is the scope would be Heath IT user interface engineering for software not considered part of a medical device.Read More
Schedule Discussion with John F. Murray, Jr.
John is currently providing telephone and face-to-face meetings to discuss: Cybersecurity, Part 11, 483 Response, design controls expectations for software documentation, and other topics.
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