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FDA

perrigo

Perrigo Announces FDA Final Approval For Generic Rogaine

Allegan-based Perrigo Co. has received final approval from the United States Food and Drug Administration for its abbreviated new drug application for over-the-counter Minoxidil Foam, a generic version of Men’s Rogaine Foam

WWJ Newsradio 950–05/02/2011

perrigo

FDA Clears Perrigo Allegan Manufacturing Plant In Re-Inspection

Allegan-based Perrigo Co. announced that it had achieved “acceptable regulatory status” in a re-inspection of its Allegal manufacturing plant by the Detroit office of the United States Food and Drug Administration.

04/12/2011

(credit: faygocupcakes.com)

FDA: Link Between Food Coloring And Hyperactivity?

The Food and Drug Administration wants to know if there could be a link between the artificial food coloring and hyperactivity in children.

WWJ Newsradio 950–03/31/2011

The Terumo Advanced Perfusion System 1, introduced in 2003

Terumo Reaches Agreement With FDA On Quality System Improvements

Terumo Cardiovascular Systems, an Ann Arbor-based subsidiary of Terumo Corporation of Tokyo, Japan, announced it has agreed to the terms of a consent decree with the U.S. Food & Drug Administration regarding quality system improvements at the company’s Ann Arbor plant.

03/22/2011

Limited Skippy Peanut Butter Recall

If you are just settling in to enjoy your peanut butter sandwich, please check the label to make sure you are not affected by the latest recall.

WWJ Newsradio 950–03/05/2011

neogen

Neogen’s Tests for Salmonella In Feed Meet FDA Draft Guidance

Lansing-based Neogen Corp. (Nasdaq: NEOG) announced that its rapid tests for salmonella meet the guidance for salmonella in animal feed currently being considered by the United States Food and Drug Administration.

01/25/2011

neogen

Neogen’s Rapid Test for Salmonella Receives FDA Approval

Lansing-based Neogen Corp. (Nasdaq: NEOG) Wednesday announced that its rapid test for Salmonella enteritidis has been determined by the United States Food and Drug Administration to be equivalent to the FDA’s traditional testing method in accuracy, precision, and sensitivity for detecting SE.

01/12/2011

cigs-getty

FDA: Agency Must Review Tobacco Products

The Food and Drug Administration says it must review tobacco products that were introduced or changed over the last four years in order for companies to keep selling them.

WWJ Newsradio 950–01/05/2011

Medical Device Reprocessor Opens

The Midwest Reprocessing Center announced the opening of its new  FDA-registered location in Saginaw for the reprocessing of non-invasive single-use medical devices such as compression sleeves, blood pressure cuffs and pulse oximeters. MRC’s processes, which […]

12/22/2010

FDA Reviews 2 New Drugs To Reduce Prostate Cancer

Health regulators said Monday that two drugs from GlaxoSmithKline and Merck reduce the risk of prostate cancer in men, though scientists questioned the drugs’ overall benefit, since the tumors they prevent are usually not life-threatening.

11/29/2010

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