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Food supplements in Europe are subject to the Directive 2002/46/EC (or "Food Supplements Framework Directive") but also to national laws that are specific to each EU state.
The Biocidal Products Regulation (BPR) EU No. 528/2012, aims to control biocidal products, limiting as much as possible the risks they may pose to human health and the environment.
The European Regulation 2017/745 or MDR replaces the old directives and standardizes the obligations of the various economic operators in the medical device (MD) industry in Europe.