Medical Device Regulation – focusing on the unique device identifier
Regulation 2017/745 EU introduces measures supporting transparency and traceability in the field of medical devices. More specifically, a unique device identifier –...
Regulation 2017/745 EU introduces measures supporting transparency and traceability in the field of medical devices. More specifically, a unique device identifier –...
In this moment of uncertainty, linked to the unknown evolution of the COVID-19 pandemic, and to the stop to all...
Pharmaceutical legislation ensures the quality and safety of medicines through the compliance with regulations and strict controls on all manufacturing steps as...
In this particular period, with the pandemic changing our daily life and our habits, pets have become more important. Therefore,...
The surveillance of patients’ and consumers’ safety concerns products that are very different one from the other: medicines, medical devices,...
In the last decades, the World Health Organisation repeatedly invited countries all over the world to implement regulatory policies and...
The registration of a trademark can be a winning strategy to promote one’s products or services over those from other...
The Official Journal of the Italian Republic is an essential tool in the pharmaceutical sphere: in fact, any authorisation, change, variation, cancellation...
In the latest years, the consumers’ interest for the information reported in the labelling of food products grew so much that the...