Commission committees list EU risk assessment courses
This article was originally published in Clinica
Executive Summary
The European Commission’s scientific committees have published a list of risk assessment training schemes which include courses that are of relevance to the medical devices sector. The list is heavily dominated by courses on offer in the UK, but also includes some held across the EU. One course is specifically aimed at nanotechnology and its ethical implications in the Netherlands; there is also a course on public health protection in the UK. The list is available at: http://ec.europa.eu/health/dyna/training/training_en.cfm
You may also be interested in...
EU Regulatory Roundup, March 2024: Busy Agenda In Broad Range Of Key Areas
March was an important month for EU medtech regulation with an interesting spread of news relating to the Medical Device and IVD Regulations, the Batteries Regulation, the Artificial Intelligence Act and more.
EU’s Revised Phthalates Guideline Features New Annexes Focused On Alternatives
The effects of phthalates, plasticizers used in many medical devices, on the human endocrine system, have long been debated. But how safe are the alternatives? Updated guidelines give more insight.
Non-Medical Brain Stimulation Devices: Could They Be Down-Classified Again In the EU?
Six types of products that do not have an intended medical purpose fall under the scope of the Medical Device Regulation. Understanding their risks is complex and subject to regular re-examination by the European Commission.