Testing and Evaluation Strategies for the Biological Evaluation of Medical Devices submitted for CE Mark and FDA Approval

Download UL Article covering Biological Safety strategy for Medical Devices

UL experts from the EU and US provide an overview of the requirements for non-clinical test data for EU and US submissions.

 


For support with your non-clinical testing strategy and reports, please contact UL at:  1-888-503 5537, or email UL at Medical.Inquiry@ul.com  or Click here for a list of regional contacts.

 

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