Scrip is part of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

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
UsernamePublicRestriction

Austrian MEP raises concerns over medtech regs ahead of first draft of recast

This article was originally published in RAJ Devices

Executive Summary

A member of the European Parliament has put forward some key questions about "dangerous medical devices, in particular implants", the answers to which are likely to influence the views of parliament ahead of it receiving a first draft of the proposed recast of the medical device directives1. The draft is expected to be available in the first half of 2012.

You may also be interested in...



Interview: Bassil Akra Speaks About Leaving TÜV-SÜD, Future Challenges, Opportunities And COVID-19 Realities

As Bassil Akra returned his office equipment and access card to his TÜV-SÜD offices in Munich amidst a welcome of balloons, Medtech Insight asked what this meant for him personally and what it will be like to start in consultancy during a pandemic.

EU MDR Panel Discussion: Why An Extra Year Is Not Really A Delay For The MDR – How To Survive Changing And Confusing Times

26 May 2020, the date that the Medical Device Regulation was originally due to apply in the EU, was a good time to take stock of where the medtech sector finds itself. Three of the most renowned and outspoken experts on the EU medical device regulatory system gave their views in this exclusive interview.

Commission Allows Notified Body Designation Renewals Without On-Site Visits

National authorities can renew notified body designations by conducting reviews that do not include on-site visits, overturning one of the most critical measures introduced in medical device regulations over the last seven years.

UsernamePublicRestriction

Register

SC142222

Ask The Analyst

Please Note: Click here for more information on the Ask the Analyst service.

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