Understanding the CE Marking process for In Vitro Medical Devices – 1 day course
What you will know by the end of the course:
The course will give you a wide understanding of the In Vitro Medical Device Directive (IVDD 98/79/EC) and how it applies to your medical device application.
Following the course, you will understand how to fulfil the Essential Requirements and how to create a compliant product Technical File.
A training course is in development that will enable you to interpret and understand the up-coming IVDR and will be completed once the IVDR is released (expected May 2017). The IVDR course will be available by late-2017.
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