The date of application of Regulation EU 745/2017 (hereafter MDR, 26 May 2020) is close and Medical Device (MD) manufacturers shall be...
Medical Device manufacturers shall soon face relevant changes as provided for by the new European Regulation requiring, among other novelties,...
The 13th italian national meeting of pharmaceutical qualified persons (QP) was held last 28 November. The speeches of the AIFA officers Dr....
In 2014 the European Parliament approved the Regulation on clinical trials on medicinal products for human use (Regulation 536/2014) with...
“New strategies for medical device assessment” is the title of a workshop presented in Rome on 4 October by Di Renzo...
The US Food and Drug Administration has just launched an alert on the vulnerability of medical devices to hackers’ attacks, that...
Great masters teach that the more you know a subject, the more easily you will be able to explain it....
The still uncertain situation of the exit of United Kingdom from the European Union is having negative effects on the economies of...
The Italian Ministry of Health has published new information to clearly report the labelling requirements to be complied with for food supplements containing...
