By Stewart Eisenhart, Emergo Group
Medical device regulators in France have published new information for manufacturers on how to adjust to an expected decline in Notified Bodies in Europe due to more stringent CE Marking and quality auditing requirements in the near future.
Get the full story here at the Emergo Group’s blog.
The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees.
The post French Competent Authority provides roadmap for manufacturers as European Notified Body numbers decrease appeared first on MassDevice.
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