We are excited to welcome Nirjit Nahal to our team as a Quality Systems Specialist. Nirjit brings a wealth of experience in the medical device industry, where
Manufacturers of class Ir surgically reusable devices are, under the MDR (EU 2017/745), required to submit documentation to a Notified Body to review reprocessing aspects of their
With less than a month to go, the clock is ticking for the next critical deadline, 26th September 2024, for legal manufacturers of legacy devices (class I
The recent EU commission publication (EU)2024/1860 aims to address the following: Accommodate the future roll-out of Eudamed modules – timeline for mandatory use of each module once
