Skip to main content

Blog

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, …

Basics of Unique Device Identification (UDI)

What is UDI?  An UDI is a distinct numeric or alphanumeric code used to identify medical devices throughout …

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: …

Technical Documentation – Future proof and save time/costs

Technical Teams often produce a large percentage of their documents and Inefficiencies are introduced when teams cre…

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 proce…

CONNECT WITH US

    Subscribe
    The First Step

    Let's talk about how DDi can help you