The European Commission issued a proposal to restrict microplastics. The regulation will have an impact on products containing those substances. Read more!
The European Commission issued a proposal to restrict microplastics. The regulation will have an impact on products containing those substances. Read more!
Discover the effects of the implementation of MDR on the EU medical device market and the most relevant challenges in our new article!
Medical devices that have obtained CE Certificate under the MDD 93/42/EEC can circulate in the EU market. Learn the conditions here!
Join our latest Webinar about the EU IVDR vs. the Swiss IVDO.
Watch the recording to discover all the details from our expert!
On June 27, 2022, the Health Products Regulatory Authority (HPRA) published an alert about the serious health risks linked to the substance Melanotan 2. Read all the details!
The Spanish competent authority has updated its instructions for requesting authorisation for commercialising personal care products. Visit our page for more details!
If you are unsure of how you should now proceed in order to import new devices or maintain the previous ones in the European territory, this webinar is what you were looking for! Register now!
In January 2022, the Journal of the European Union published harmonised standards for medical and health care products, including symbols that manufacturers must provide for their products. Read all the details!
Join our latest Webinar about EUDAMED. Sandra Ferretti, CCO at Obelis Group will walk you through all the challenges related to Actor and Device Registration!
Rapid antigen tests are widely used in the European Union and are helping to strengthen many countries testing capacities. For more information visit our page!