It has been more than a decade since proposals were first made to reform the long-standing General Product Safety Directive (GPSD) in Europe. A lot has happened since then, and as of this week, we now have a new General Product Safety Regulation on the books to replace the GPSD.
Regulating the Digital Sector, Transforming Consumer Protection Regulation – UK Government Proposes Significant Reforms With Draft Bill
We finally have sight of the long-awaited Digital Markets, Competition and Consumers Bill. Warning: It is a sizeable and ambitious piece of legislation, but the following is our summary take on the key competition and consumer issues.
On 19 April 2023, the European Parliament formally approved a new European Union Deforestation Regulation on commodities and products associated with deforestation and forest degradation.
The European Commission recently published its proposal for a new Directive on common rules promoting the repair of goods. In this blog we take a look at the proposals and why they matter for companies doing business in the EU.
Breaking news: The European Parliament has this morning overwhelmingly approved the text of the new General Product Safety Regulations. This new legislation is a significant overhaul of the rules governing the safety of consumer products in the EU
On the 23 March 2023, the European Commission proposed a new Green Claims Directive (the “Directive”). If adopted, the Directive will have a huge impact on businesses making green claims on the products they sell in the EU.
The Council of the European Union votes in favor of amending the transitional provisions in the MDR and IVDR
The extension of the transitional periods in the MDR and the removal of the “sell-off” deadline in the MDR and the IVDR were approved by the Council of the EU today. The proposed legislative amendment, however, will not enter into force until it is signed by the European Parliament and the Council and published in the Official Journal of the EU.
EMA launches pilot program for expert panel scientific advice in relation to certain high-risk devices
Ten medical device and IVD developers will receive free advice on their clinical development strategies from medical device expert panels. The pilot program aims to help EMA with the implementation of the expert panel advice procedure established in MDR and IVDR.
The European Parliament votes in favor of amending the transitional provisions in the MDR and the IVDR
The European Parliament approves the European Commission’s proposal to extend the transitional periods in the MDR and remove the “sell-off” deadline in the MDR and IVDR.
The proposed EU restriction of per-and polyfluoroalkyl substances was published on 7 February 2023. If adopted into law, the restriction will result in a ban on the manufacture, use and placing on the EU market of around 10,000 PFAS,