We are thinking about using Wrike as a part of our QMS (Quality management system) for medical device development according to ISO13485:2016. Have anyone to your knowledge validated your software for this? If not would you be interested in the results of our validation and user story when using it for medical device development?
For validation we will be using paragraph 4.2.5 & 4.1.6 in ISO13485:2016 standard.
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