Hi @Anonymous ,
Thank you for the information. As I understand the ISO requirement you noted, the validation is part of the procedural process, or plan, that you will need to set up, and is not provided by the manufacture of the software. It sounds like this will include a review process of the features and output of the software as needed for your use.
I found the following links that may shed some light on the process:
http://www.fda.gov/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm085281.htm
http://www.fda.gov/downloads/medica...onandguidance/guidancedocuments/ucm073779.pdf
Please let me know if this information helps.
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