News UK health secretary promises to tighten regulatory procedures for medical devices BMJ 2012; 345 doi: https://doi.org/10.1136/bmj.e7192 (Published 24 October 2012) Cite this as: BMJ 2012;345:e7192 Article Related content Metrics Responses Peer review Related articles Feature The truth behind “made in Europe” labels on medical devices Published: 24 October 2012; BMJ 345 doi:10.1136/bmj.e7193 Feature Manufacturers offered helping hand with EU approval Published: 25 October 2012; BMJ 345 doi:10.1136/bmj.e7225 FeatureFaulty hip implant shows up failings of EU regulationEditorialThe scandal of medical device regulationFeatureHow a fake hip showed up failings in European device regulation See more Individual care plans reduce falls and broken hips in New Zealand hospitals BMJ December 05, 2016, 355 i6490; DOI: https://doi.org/10.1136/bmj.i6490 Bill to boost medical research funding and speed drug approval passes US house BMJ December 01, 2016, 355 i6498; DOI: https://doi.org/10.1136/bmj.i6498 Workloads threaten to undermine doctors’ training, GMC finds BMJ December 01, 2016, 355 i6495; DOI: https://doi.org/10.1136/bmj.i6495 Junior doctors’ low morale is putting patients at risk, Royal College of Physicians warns BMJ December 01, 2016, 355 i6493; DOI: https://doi.org/10.1136/bmj.i6493 Funds are not reaching frontline services BMJ November 28, 2016, 355 i6273; DOI: https://doi.org/10.1136/bmj.i6273
