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CE Marking

CE Marking



Location:Netherlands
 
Description:A successful Biotech company is looking for a regulatory consultant with previous experience with medical device regulatory affairs for In Vitro diagnostic medical devices (reagents and software).
The company develops sequencing based (companion) diagnostics and software. The consultant will provide advice to achieve and maintain CE marking(s) for the devices under the IVD directive for new products.
 
Requirements:Regulatory consultant with experience in CE marking
 
Keywords:companion diagnostics, regulatory affaires, CE marking
 
Delivery time frame:short term
 


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