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.
News
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.
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).
Children’s safety ensured: an evaluation of the Toys Safety Directive by the European Commission
Find out more about the evaluation by the European Commission on the Toys Safety Directive.
Final SCCS Opinion on the safety of presence of BPA in clothing articles published
The EU Commission and its Scientific Committee on Consumer Safety (SCCS) published its final opinion on presence of Bisphenol A (BPA) in clothing articles.