Scrip is part of the Business Intelligence Division 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

Recast will seek to better define scope of EU medtech directives

This article was originally published in RAJ Devices

Executive Summary

One of the key aims of the European Commission in the recast of the medical device directives it is working on is to ensure that there is better clarity than there is at present about which products are and are not regulated under the directives. Areas of focus include products on the borderline with other directives, as well as implantables or other invasive devices without a medical purpose.

Advertisement
Advertisement
UsernamePublicRestriction

Register

SC096662

Ask The Analyst

Please Note: You can also Click below Link for Ask the Analyst
Ask The Analyst

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