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

Click here for the full article on Global Regulatory Press.

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