Regulation on Medical Devices (MDR)

Mark Cusworth, PRISYM ID, examines EU Medical Device Regulation and its implications on labeling – and looks ahead to a Christmas future that could become a nightmare unless companies act now. more

17 Nov 2017 10:38 Features

The BSI’s UK & Ireland Medical Devices Regulatory Seminars in November are for all medical device manufacturers, regulatory affairs and quality assurance staff. more

23 Oct 2017 15:37 News

Global public health and safety organisation NSF International recently completed the acquisition of Prosystem, a German medical device consulting firm specialising in regulatory affairs and clinical evaluation. more

10 Oct 2017 09:45 News

The British Standards Institution (BSI) tells Med-Tech Innovation why it developed Compliance Navigator – a workflow tool that takes the leg-work out of managing medical compliance. more

4 Oct 2017 13:57 Features

Here’s ten things you really need to know about the new European Medical Device Regulation. more

29 Sep 2017 10:19 News

Engineering and scientific technologies company, Renishaw, will be exhibiting at the Digital Symposium at Swansea University on 29 June as part of its event, “Digital Futures in Health and Wellbeing: can public services survive without them?”. more

27 Jun 2017 11:30 News

Quality provider InfinityQS has argued that the medical device industry must develop a common language within its data systems to ensure full legal compliance and internal traceability. more

27 Jun 2017 10:45 News

Maetrics reveals the practical implications for medical device manufacturers and how to address them as the new MDR comes into force. more

1 Jun 2017 12:13 News


Alexandra Lande /

The medtech sector has welcomed the vote from the European Parliament to endorse new regulations on in vitro diagnostic medical devices (IVDR) as well as the new Regulation on Medical Devices (MDR). more

10 Apr 2017 16:38 News