ANSES brings off an unprecedented assessment of the types and composition of tobacco and vaping products sold on the French market under the new European regulatory framework.
ANSES brings off an unprecedented assessment of the types and composition of tobacco and vaping products sold on the French market under the new European regulatory framework.
The EU Chemical Strategy for Sustainability aims to build a zero-pollution environment in line with Europe’s new agreement towards a toxic-free Union: The Green Deal.
The Italian Ministry of Health published first report on the surveillance activity it carries out on medical devices to ensure only safe and effective devices are circulating on the national territory.
The Kanavape Case (C-663/18) judgment provides some much-needed clarity over the status of CBD in the EU and whether it should be classified as a narcotic substance.
Electronic cigarettes and any e-liquid containing nicotine are subject to the discipline set out by the Tobacco Products Directive 2014/40/EU (TPD).
European Motor Vehicle Regulation 2018/858 entered full effect in September 2020. Talk to our EU regulatory experts about your vehicle or product's compliance.
The MHRA has released its latest guidelines for medical device requirements for products in Great Britain, Northern Ireland, and Europe from January 1st 2021.
The European Commission has issued market and compliance guidance on regulatory requirements for manufacturers of medical face masks.
Germany established NAKI, the National Working Group for the Implementation of the new EU Regulations on MDR IVDR. Read all the details in this article!
All radio equipment, including its embedded software, must comply with the Radio Equipment Directive 2014/53/EU (RED). Find out all the details here!