Fda

(MENAFN - PR Newswire) ADDISON, Ill., March 24, 2025 /PRNewswire/ -- Huntleigh Healthcare is proud to announce that the world-renowned Dawes-Redman CTG Analysis TM has been approved for use in ... .

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FDA-Approved Artificial Blood Vessel Stirs Concerns

New York Times 24 Mar 2025

The F.D.A. approved an artificial vessel to restore blood flow in patients, despite its own scientists flagging questionable study results and potentially fatal ruptures of the product ... .

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Biocon subsidiary secures FDA approval for critical blood pressure medication

Business Line 24 Mar 2025

Food and Drug Administration (FDA) approval for its Abbreviated New Drug Application (ANDA) for Norepinephrine Bitartrate Injection USP, the company announced today ... pharmaceutical market ... ....

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Cheese sold at Michigan Aldi stores recalled. Why FDA says you should throw it out

Detroit Free Press 24 Mar 2025

Exposure to the contaminants may cause temporary health risks with an unlikely chance of serious adverse health consequences, the FDA reported ... Expiration dates from July 13 and 14, 2025, and a bar number of 4061463330840, according to the FDA.

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Agilent xCELLigence RTCA Instrumentation Applied in Recent FDA Approval (Agilent Technologies Inc)

Public Technologies 24 Mar 2025

A) is pleased to announce its role in supporting Autolus Therapeutics' FDA approval for AUCATZYL®, a recently approved CAR T therapy ... Autolus in achieving the high standards required for FDA approval.

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FDA-Approved Artificial Blood Vessel Stirs Concerns

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