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eIFU Requirements Under the EU MDR and Regulation 2021/2226
What is an eIFU?
In general, an eIFU is defined as a non-paper version of the instructions for use. Currently, the definition of an eIFU is not the same in each market.
In the EU, accordin…

eIFU for Medical Devices: Country Specific Regulations and Benefits
There are several benefits of using electronic Instructions for Use (eIFU) labeling for medical devices, including:
1. Accessibility: eIFUs can be accessed from anywhere with an internet connec…

Authors hate this and companies should respond
Where do authors spend most time that they hate. Easy guess, it’s Formatting and reviews.
In spite of process documents, templates, rule books, qc checklists, authors still spend lot of t…
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