European Commission's revision of EU Machinery Directive expected in the second quarter of 2021. It's set to clarify definitions of new digital technologies.

European Commission's revision of EU Machinery Directive expected in the second quarter of 2021. It's set to clarify definitions of new digital technologies.
Obelis' CE marking experts walk you through the simple 7-step process for obtaining a CE marking for medical devices and accessing the European market.
European Commission issues special notice to medical and in-vitro diagnostic device manufacturers to clarify scope and requirements of new EU regulations.
European Chemicals Agency releases a report on truthfulness of data on nanomaterials in EU cosmetics products. Download the report for free in English.
Learn more about the definition and categorization of incidents as outlined by new EU medical device regulation 2017/745.
March 29th 2019 is fast approaching, and the UK is currently facing to leave the EU without a deal in place. For this reason, the UK government has been publishing technical notices for businesses and citizens to understand what to expect in a no deal scenario. We will focus on the recently published MHRA official guidance with regard to the regulation of medicines, medical devices and clinical trials in case there is no Brexit deal. Find here the most remarkable points.
Authorities in the Netherlands classify the printing of misleading claims on labelling or instructions for use on cosmetics products a criminal offence.
European Commission publishes updated version (V1.20) of the Borderline and Classification Manual for medical and in-vitro diagnostics devices on the EU market.
The Poison Centres website has been updated with new support pages in order to assist the industry to prepare and submit information on hazardous mixtures.
Superior Health Council (SHC) publish report on associations between breast implants and anaplastic large cell lymphoma. Discover the results with Obelis.