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IMUNON'S IND Application Cleared To Begin Human Testing Of IMNN-101

IMUNON'S IND Application Cleared To Begin Human Testing Of IMNN-101
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Imunon, Inc.: IMUNON's IND Application Cleared to Begin Human Testing of IMNN-101

Imunon, Inc.: IMUNON's IND Application Cleared to Begin Human Testing of IMNN-101
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Business News: Moderna releases new data on Covid breakthrough cases it says supports need for booster shots

Moderna releases new data on Covid breakthrough cases it says supports need for booster shots : Rashtra News A healthcare worker fills a syringe with Moderna COVID-19 vaccine at the Giorgio Companies site in Blandon, PA where the CATE Mobile Vaccination Unit was onsite to administer Moderna COVID-19 Vaccines to workers Wednesday morning April 14,

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FDA Panel Members Who Voted on Abbott's Heart Device Had Financial Ties to Company

FDA Panel Members Who Voted on Abbott's Heart Device Had Financial Ties to Company
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FDA: Trivalent Influenza Vaccine Formulation Back for 2024-2025 Season

The decision was based on surveillance data indicating that there have been no confirmed detections of circulating B/Yamagata lineage viruses after March 2020.

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Worldwide Embalmer Blood Clot Surveys Show Possible Link to Covid Vaccines

Worldwide Embalmer Blood Clot Surveys Show Possible Link to Covid Vaccines
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CSL Seqirus prepared to deliver 2024/25 U.S. season influenza vaccine portfolio

The vaccine portfolio is based on the trivalent strains recommended by the FDA's Vaccines and Related Biological Products Advisory Committee.

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FDA Roundup: March 22, 2024

FDA Roundup: March 22, 2024
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FDA Roundup: March 22, 2024

/PRNewswire/ -- Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: Today, the FDA issued an...

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FDA Roundup: March 22, 2024

FDA Roundup: March 22, 2024
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