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

This article was originally published in SRA

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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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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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