A definitive guide to CE marking in Europe. Discover what a CE marking is, what products require a CE mark, and why a CE mark is required on the EU market.

A definitive guide to CE marking in Europe. Discover what a CE marking is, what products require a CE mark, and why a CE mark is required on the EU market.
The new EU Regulation on in vitro diagnostic devices (IVDR), applicable since May 26, 2022, affected the classification and compliance process of COVID-19 tests.
The EU proposal aims to introduce new hazard classes based on scientific criteria for endocrine disruptors as well as other chemicals which can accumulate in living organisms or enter the water cycle.
In November 2022, the Belgian government notified the EU of a draft Royal Decree to limit the placing on the market of single-use plastic products. Read all the details in our article!
There was a general agreement between the Council of the EU representing the EU Member States and the European Commission to extend the transitional period (legacy period) to the Medical Devices Regulation (MDR). Read all the details in our article!
Find all data collected and results from the Italian National Registration for Breast Implants pilot phase. Read it now!
Vigilance and Post-Market Surveillance definition, differences and their scope. Visit our webpage for all the details!
The European Commission issued a proposal to restrict microplastics. The regulation will have an impact on products containing those substances. Read more!
One more step is taken towards a common charger in the EU for all electronic devices. Learn more!
The Commission published a new legislative proposal for a Regulation on new Ecodesign requirements. Visit our webpage for all the details!