A single word change in EU legislation — “may appoint” became “shall appoint” — has turned the EU Authorized Representative from an optional administrative step into a mandatory requirement for many non-EU manufacturers. Here’s what an EU AR actually does, why the 10-year documentation rule matters, and how F2 Labs’ new EU Authorized Representative Service helps you stay compliant.
As both established and startup consumer electronics manufacturers look to expand their market reach, the European Union presents an enticing, lucrative growth opportunity. Entry into this market comes with its
The COVID-19 pandemic has thrown us all for a loop. Effects of the pandemic have been seen across many industries, supply chains, and more, including the extension of deadlines for
F2 Labs is officially an ASCA-accredited testing laboratory! We are one of only 17 labs approved by the FDA. This program will help increase product safety for the end-user and shorten the time it takes for FDA approval of your product.
This is the first time in history that the FDA has had a list of approved labs. F2 Labs is officially an ASCA-accredited testing laboratory.
The UK has left the EU and new rules concerning the transition for most CE products to UKCA products began in January 2021. The transition period for most products ends
