The sale of food supplements in Italy, through either traditional channels or online, is steadily growing and many companies are...
The transition from the old Directive on in vitro diagnostic medical devices 98/79/EC (IVDD) to the new Regulation 2017/746 (IVDR), which will apply from...
The Italian Ministry of Health has published a communication on their portal, regarding an action by the NAS, the special...
The title is not wrong, the new European Regulation on medical devices 2017/745 (MDR) is already causing problems to manufacturers, or better said up to now to...
The Italian Ministry of Health has updated its website reporting the appropriate procedures to be followed to apply for the authorisation of advertisements of medicinal products...
The Ministry of Health published a memorandum letter to define the maximum intake limit for caffeine as well the properties associated with this ingredient...
The Italian antitrust authority (AGCM) has fined three companies located in Portugal, Slovenia and in the United Kingdom for a...
Parallel imports of medical devices is a concept transferred de facto to the medical sector from the pharmaceutical one. The underlying activity...
There is a predictably puzzling issue related to class I medical devices according to the present and old Directive 93/42/EEC (MDD) that will be...
