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eIFUs and animal tissues in devices: UK seeks feedback on EU rules

This article was originally published in SRA

Executive Summary

The UK Medicines and Healthcare products Regulatory Agency is inviting feedback on how it should implement into UK law two EU regulations on: using electronic instructions-for-use (eIFUs) with certain devices, and introducing precautionary measures for devices manufactured using non-viable tissues from Transmissible Spongiform Encephalopathies (TSE)-susceptible species1,2.

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