Guidance on Classification Rule for in vitro Diagnostic Medical Devices aims to uniformly apply the classification rules stated in the new regulatory framework

Guidance on Classification Rule for in vitro Diagnostic Medical Devices aims to uniformly apply the classification rules stated in the new regulatory framework
European Commission’s European Green Deal aims at transforming production and consumption of products on the EU market, in order for them to become more durable, resilient and eco-friendly.
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.
Data transfer from the EEA to third countries -The finding of an adequate level of protection. The protection of personal data and its interaction with the MDR and IVDR
In this webinar, we will be addressing the new Regulation on Market Surveillance & Compliance of Products to assist online sellers in their compliance path:
Through this interview, you will get more insight about Obelis. What are doing and how can we help you to compliance with EU regulations.
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).