Europe - December 2017
EU: Codes and corresponding device types, application forms, and application documentation drafted for NB designation
EU: Products whose principal intended action (depending on PAC present in cranberry) is to prevent or treat cystitis, are not medical devices
France: Temporary Specialised Scientific Committee set up to address cybersecurity issues in medical device software
UK: MHRA issues guidance on new European medical device and IVD Regulations
UK: MHRA publishes guidance on human factors and usability engineering
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