![If The EU MDR Is Product Compliance's Future - Be Afraid, Be Very Afraid! [Podcast]](https://qualityinspection.org/wp-content/uploads/2021/07/IfTheEUMDRIsProductCompliancesFuture-BeAfraidBeVeryAfraidPodcast-1000x445.jpeg)
In this episode... Renaud Anjoran is joined again by Clive Greenwood, an expert in product compliance for a new episode following on from the first episode they recorded about product compliance (which covered the main compliance challenges faced by importers). This time they're looking at the future of compliance standards by examining the new Medical Device Regulation (EU) 2017/745 (MDR), an extremely comprehensive and stringent regulation. They believe this 'MDR' signposts how future … [Read more...]
New EU Medical Device Regulation: No More Traders?
If you have been buying China-made medical devices and reselling them in the European Union, and if you haven't actually done the product development work yourself, can you keep doing that business now that the new EU medical device regulation changes have come into effect? In many cases, no. … [Read more...]