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Fresenius looking to boost output after hurricane damage at rival Baxter

UPDATE 4-Fresenius looking to boost output after hurricane damage at rival Baxter Updates Oct 8 story to add additional Fresenius comment, paragraph 4 FRANKFURT, Oct 9 (Reuters) - Germany's Fresenius FREG.DE said it was checking options to speed up the start of new production lines of medical equipment at a North Carolina facility to help mitigate potential shortages from hurricane damage to rival Baxter's BAX.N site in the same state.
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Fresenius looking to boost production after hurricane damage at Baxter

Fresenius looking to boost production after hurricane damage at Baxter FRANKFURT, Oct 8 (Reuters) - Germany's Fresenius FREG.DE said it is checking options to start new infusion-solution production lines faster than planned at a North Carolina facility to help mitigate potential shortages due to the impact of Hurricane Helene on rival Baxter's North Cove site in the same state.
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Fresenius: mAbxience And Teva Announce Second Strategic Global License Agreement For Biosimilar Oncology Treatment Candidate

BRIEF-Fresenius: mAbxience And Teva Announce Second Strategic Global License Agreement For Biosimilar Oncology Treatment Candidate Oct 3 (Reuters) - FRESENIUS SE & CO KGAA FREG.DE : MABXIENCE AND TEVA ANNOUNCE SECOND STRATEGIC GLOBAL LICENSE AGREEMENT FOR BIOSIMILAR ONCOLOGY TREATMENT CANDIDATE FRESENIUS SE - AGREEMENT COVERS GLOBAL MARKETS, INCLUD
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FDA Says Identified Fresenius Kabi USA's Recall For Correction Of Ivenix Infusion System Lvp Software As Most Serious Type

BRIEF-FDA Says Identified Fresenius Kabi USA's Recall For Correction Of Ivenix Infusion System Lvp Software As Most Serious Type Oct 1 (Reuters) - FDA: FDA: FRESENIUS KABI USA, LLC, ISSUES CORRECTION FOR IVENIX INFUSION SYSTEM LVP SOFTWARE DUE TO ANOMALIES THAT MAY CAUSE DELAY/UNDERDOSAGE OF THERAPY FDA: IDENTIFIED FRESENIUS KABI USA'S RECALL FOR C
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Formycon And Fresenius Kabi Receive FDA Approval For Fyb202/ Otulfitm

BRIEF-Formycon And Fresenius Kabi Receive FDA Approval For Fyb202/ Otulfitm Sept 30 (Reuters) - FORMYCON AG FYB.DE : AND FRESENIUS KABI RECEIVE FDA APPROVAL FOR FYB202/ OTULFITM(USTEKINUMAB-AAUZ) TULFITMRECEIVED FDA APPROVAL FOR BOTH SUBCUTANEOUS AND INTRAVENOUS FORMULATIONS, TO TREAT SAME CONDITIONS AS STELARA® APPROVAL REPRESENTS THIRD SUCCESSFU
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