The BPR requirements for inclusion of suppliers in the Article 95 list are often confused with those for approval of a biocidal active substance. We try to clarify the difference.

ISO 10993-18:2020 is now official and sets the framework for chemical characterization of medical device materials in connection with biocompatibility evaluation within the risk management process.

The European Commission has approved a corrigendum to the Medical Devices Regulation (MDR) that includes a transition period for certain class 1 devices.

If you consume hemp products there is an increased risk of exposure to the psychoactive substance delta-9-tetrahydrocannabinol, says the European Food Safety Authority, EFSA.

Close to 45% of reported hazardous mixtures were found to be non-compliant in some way. This is the findings of an EU-wide Enforcement Forum project on classification and labelling of mixtures.

A project concerning substitution of tin-based catalysts in antifouling paint has been successful in developing viable alternatives.