09/2023 - LUXEMBOURG CHANGES TO PRODUCT INFORMATION

03/2023 - Medical Device Actors in Belgium - new system for fees 

07/2022 - Industry Single Point of Contact (i-SPOC)

06/2022 - DADI Project for Medicinal Products

04/2022 - NEW RULES on THE CONTENT & LABELLING of GREEN TEA CATECHINS

02/2022 - INTEGRATION OF EUDRAGMP WITH OMS 

SInce 28/01/2022 the OMS system of EMA has been integrated in EudraGMP.

02/2022 - UDI VS UFI - SAY WHAT? 

UDI and UFI are unique identifiers which are mandatory for Medical Devices and Dangerous Mixtures respectively.

01/2022 - EU BANS TITANIUM DIOXIDE IN FOOD SUPPLEMENTS 

In May 2021 EFSA concluded that the food additive TiO2 (E171) can no longer be considered safe when used as a food additive.