Medtech Insight 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

US PMA no more of a safeguard than EU CE mark yet drawbacks significant, report finds

This article was originally published in Clinica

Executive Summary

The US FDA's premarket authorisation system for regulating high-risk medical devices not only delays patients' access to potentially life-saving technologies but does not safeguard them against risky products any more than the EU's CE marking process.

Advertisement

Topics

Advertisement
UsernamePublicRestriction

Register

MT099406

Ask The Analyst

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

All set! This Question has been sent to 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