Medtech Insight is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

Europe’s MRI sector waits on directive rethink

This article was originally published in Clinica

Executive Summary

Of all the ill-conceived and backward-thinking EU directives, the Physical Agents Directive (Directive 2004/40/EC), also known as the EMF Directive, is up there among the worst. The directive is potentially disastrous for the MRI sector as it seeks to impose strict limits on the electromagnetic field (EMF) strengths to which equipment operators can legally be exposed. While moves to protect workers from over-exposure to EMFs are to be welcomed, the directive is so restrictive that it could prevent healthcare staff caring for patients during a scan, put an end to interventional MRI procedures, and prevent radiologists from being properly trained. It could also affect MRI research, leading to a brain drain from the EU to the US and Asia.

You may also be interested in...



Report Digest: Discussing What's Going On With Prostate Cancer Diagnosis And Treatment

In this edition of Report Digest, UK-based reporter Barnaby Pickering talks about the prostate cancer diagnostics and minimally invasive treatments markets with analyst Phil Greenfield. The two discuss ongoing developments in both treatment and diagnosis, while exploring driving and limiting factors for both.

Using Digital Tools To Unpick The Adherence Problem

An ambitious five-year public-private partnership plans to tackle non-adherence to medicines by giving patients EU-wide access to regulator-approved digital drug information. One year in, progress has been made in creating an app that could do just this.

In A First, FDA Approves Radioembolization Treatment For Liver Cancer In US

Approval for Boston Scientific’s TheraSphere offers further access to the therapy that, until now, has only been available under a humanitarian device exemption.

Topics

Latest Headlines
See All
UsernamePublicRestriction

Register

MT095162

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel