The AEMPS in collaboration with STANPA published a new guide to assist in formulating and manufacturing safe raw materials and cosmetic products. More information can be found here!

The AEMPS in collaboration with STANPA published a new guide to assist in formulating and manufacturing safe raw materials and cosmetic products. More information can be found here!
The Belgian Federal Agency for Medicines and Health Products has decided to sell the Covid self-test free of charge in Belgium. More information can be found here.
SCHEER published its final conclusion regarding the connection between breast implants' safety and ALCL. Find out all the details here!
The Machinery Directive 2006/42/EC is a key piece of EU legislation that follows the ‘New approach‘ principles. Read about the new proposal to update this legislation.
Find out more information on the new requirements by MDR and BREXIT
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.
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.
Discover the new methods of evaluation through CORE-MD project on high-risk medical devices in Europe.
The digital Annual Report 2019 contains interesting figures concerning medicines and medical devices read more about it here.
Read on the Swiss Federal Council unsigned Institutional Framework Agreement (InstA).