The Ministry of health has reminded all concerned operators that since 2nd July the notification of the products classified as food...
Following some reports, the Ministry of Health has published a memorandum letter to clarify the use of terms and acronyms on...
The new Regulation on medical devices 2017/745 (MDR), that will apply from May 2020, introduces a revision of risk classes to be attributed to medical devices and...
The opportunity to focus attention on the topic of the future that awaits medical devices based on substances (for simplicity,...
Everybody knows about the Brexit issue, the exit of the Kingdom of Great Britain and Northern Ireland from the European Union. The...
The Ministry of Health has published some updated guidelines on food supplements in its website. In particular, maximum amounts of vitamins...
The current regulating framework, based on Directive 93/42/EEC, regulated the software intended by the manufacturer to be a medical device (or to be part of...
At least until May 2022 we will remain in the era of Directive 98/79/EC, started 20 years ago. Many clients ask...
One of the characteristics defining the healthcare medical devices is the high impact of technological factors. Regardless the technological level...
