Quantcast

FDA to change review process for medical devices (access required)

By: Kimberly Atkins
Published: April 28, 2010

Tags: , ,

WASHINGTON - In an effort to streamline the premarket expert panel review process for medical devices, the Food and Drug Administration has announced changes in the way data and information is discussed during public hearings on devices under review.
© Copyright 2013 Lawyers USA. All Rights Reserved.


Comments

You must be logged in to post comments.

Sign-up for alerts

FEATURED PODCAST


Lawyers USA presents Lawyers in Practice

This is the first edition of Lawyers USA's Lawyers in Practice, where we discuss the hot issues facing practicing attorneys and law firms.

In this edition, we discuss how to prevent legal malpractice claims with better communication, with Jim Calloway, director of the Oklahoma Bar Association's Management Assistance Program, and Dan Pinnington, vice-president of Claims Prevention and Stakeholder Relations at LawPRO, a professional liability carrier based in Toronto, Canada.

Visit the Legal Malpractice Monitor to listen to the podcast.

Click here to download the podcast.