News Efor
21/07/2020
Medical devices: management of hazardous substances during the transition to regulation (EU) 2017/745
Protecting human health and the environment from the risks that chemicals can pose has always been a priority for Europe. In 2007,
25/06/2020
What is the scope of IEC62304?
With changes in new technologies and the need to digitise our environments, more and more medical devices (MDs) are integrating or
17/05/2020
Hospital Information Systems (HIS): context, challenges, and opportunities in healthcare data
Healthcare institutions generate and store a vast amount of data. From the moment a patient enters a facility, they provide a sign
28/04/2020
Masks: how to access the french market
Gaining access to the European market depends on the type of mask you wish to market. Below we set out the various types of masks,
7/04/2020
Placing on the market of biocidal products
What is a biocidal product?According to the official definition, a biocidal product is:Source : Règlement (UE) N°528/20
20/02/2020
Validation of analytical procedures according to the ICH guidelines
Since 1990, the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) has been
4/02/2020
New trends in medical journals: limited use of p-values in favour of estimated indicators and confidence intervals
Why is the p-value, once so widely used, now being called into question?
2/02/2020
Food supplements and nutraceuticals
What is a food or nutraceutical supplement?The health nutrition market is constantly evolving, driven by major public health consi
