Other Industries Archives - Page 2 of 23

Wooden shelves painted in bright colors hold an assortment of vases and pots, creating a lively and decorative scene.

New General Product Safety Regulation (GPSR) Applies from 13 December 2024

From 13 December 2024, the new EU General Product Safety Regulation (GPSR) applies, requiring stricter safety measures and a Responsible Person for all products.

Kid playing with wooden colorfull blocks

New Toy Safety Regulation and the Digital Product Passport: upcoming changes for the toy industry

The update aims to address shortcomings in protecting children from toy-related risks, notably concerning hazardous chemicals.

Main regulatory developments to follow in 2024

Find out the 2024 updates regarding Medical devices, In-Vitro diagnostics, cosmetics, construction products, toys and more!

What is CE Marking?

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.

Covid tests under IVDR – How to sell them 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.

Endocrine Disruptors — The revision of the CLP Regulation

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.

A picture of different plastic packaging

Upcoming restrictions for single-use plastic packaging (PFAS) in Belgium

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!

What manufacturers need to know about the new extensions for legacy devices

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!