The role of FDA approval in drug cases.: An article from: Trial

Product Description
This digital document is an article from Trial, published by Association of Trial Lawyers of America on November 1, 1998. The length of the article is 3389 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

From the supplier: Since this is your first products liability case involving prescription drugs, you send Defendants in drug products liability cases–and any products case where the product has complied with regulatory standards (or at least has not violated any)–can effectively use the government agency, such as the FDA, as an out-of-court expert. The argument goes something like this:

Citation Details
Title: The role of FDA approval in drug cases.
Author: Patrick A. Malone
Publication: Trial (Magazine/Journal)
Date: November 1, 1998
Publisher: Association of Trial Lawyers of America
Volume: 34 Issue: 12 Page: 28(1)

Distributed by Thomson Gale
The role of FDA approval in drug cases.: An article from: Trial

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