EU medtech industry highlights areas of concern in RoHS revision proposals
This article was originally published in RAJ Devices
Three European medtech industry associations have identified several issues that they say need to be addressed regarding plans by the European Commission to include medical devices under the scope of the European directive on the restriction of hazardous substances in electrical and electronic equipment1,2.
You may also be interested in...
The international group of pharmaceutical inspectorates, PIC/S, has issued an aide-memoire and a Q&A document to support its 2018 guideline on using health-based exposure limits to assess the risk of cross contamination in shared manufacturing facilities.
Stay up to date on regulatory guidelines from around the world with the Pink Sheet's Guidance Tracker. The complete Global Pharma Guidance Tracker, with sortable and searchable listings going back to 2014, is available online.
Stay current on regulatory guidelines from around the world with Medtech Insight's Guidance Tracker. Fifty-one guidance documents have been posted on the tracker since its last update.