Find out more information on the new requirements by MDR and BREXIT
News
Webinar: Classification rules under IVDR and Covid-19 derogation lists & database
The upcoming IVDR regulation will be fully applicable as of May 26, 2022. There will be changes in the IVDR landscape, and manufacturers must make sure to be compliant on time, in order to keep selling their devices on the European market.
Webinar: Complying with the MDR
The new medical Device Regulation is fully applicable as of May 26, 2021, therefore you need to know how to manage your Legacy Devices Compliance in the EU.
Webinar: Cannabis-based ingredients use and restrictions in cosmetics for the EU market
The cosmetic industry has experienced a significant rise in the presence of cannabis-based ingredients. Find out more about restrictions and use.
Webinar: Cosmetics restrictions- Bans & Claims
Find out the cosmetic restrictions of the European Market.
EU tobacco products directive is effective after all!
Read what the first Report published by the European Commission on the Tobacco Product Directive says.
High-risk medical devices in Europe: new methods of evaluation through CORE-MD project
Discover the new methods of evaluation through CORE-MD project on high-risk medical devices in Europe.
ECHA, REACH and Animal Testing
Read more on testing and marketing bans in the EU.
FAMHP releases its Annual Report: Focus on medical devices
The digital Annual Report 2019 contains interesting figures concerning medicines and medical devices read more about it here.
Medical Device Industry: Switzerland becomes a “third country”
Read on the Swiss Federal Council unsigned Institutional Framework Agreement (InstA).