GS1 recently hosted a Scan4Safety UDI focussed webinar. Advena were present at that webinar, here are some top-level highlights from this webinar: Standards are the enabler. The
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
