Lilly reports full Q4 2024 financial results, provides 2025 guidance
Eli Lilly and Company today announced its financial results for the fourth quarter of 2024 and detailed 2025 financial guidance.
Read MoreTag Archives: U.S. Food and Drug Administration
FDA Approves Greenfield Company’s Canine Itch Medicine
Elanco Animal Health Incorporated announced the U.S. Food and Drug Administration has approved Zenreli, a highly effective and convenient once-daily oral JAK inhibitor for control of itching associated with allergic dermatitis and control of atopic dermatitis in dogs at least 12 months of age.
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Medtronic Issues Urgent Medical Device Recall For Endotracheal Tubes
The U.S. Food and Drug Administration is alerting health care providers and facilities to stop using NIM Contact EMG Reinforced Endotracheal Tubes and NIM (Standard) EMG Reinforced Endotracheal Tubes by Medtronic.
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FDA Approves Lilly’s Zepbound For Chronic Weight Management
The U.S. Food and Drug Administration approved Eli Lilly and Company’s Zepbound injection, the first and only obesity treatment of its kind that activates both glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1 hormone receptors.
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Food And Drug Administration Approves COVID Boosters For Upcoming Season
The U.S. Food and Drug Administration on Monday approved the latest round of COVID-19 boosters, as public health officials brace for another cold and flu season.
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Manchester University To Maintain New National Drug-Gene Database
Manchester University students and faculty in the pharmacogenomics, or PGx, program are taking an active role in maintaining a nationwide database that cross-references drug-gene interaction information in clinical guidelines with U.S. Food and Drug Administration data.
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Zimmer Biomet Gains FDA Clearance For First ‘Smart Knee’
Zimmer Biomet and Canary Medical jointly announced the U.S. Food and Drug Administration has cleared the way for marketing of the world’s first and only smart knee for total knee replacement surgery.
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FDA Approves Zimmer Biomet’s Fourth Robotic Implant System
Zimmer Biomet announced the U.S. Food and Drug Administration has approved clearance of the ROSA Hip System for robotically-assisted direct anterior total hip replacement.
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Kroger Health To Provide COVID-19 Vaccine Nationwide
Kroger Health, the healthcare division of The Kroger Co.announced on Tuesday it will provide the COVID-19 vaccine nationwide across its 2,200 pharmacies and 220 clinics, partnering with the federal government and state health departments to administer the vaccine in accordance with the rollout plan.
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Medtronic Receives FDA Clearance For Cement-Augmented Pedicle Screws
DUBLIN — Medtronic plc today announced U.S. Food and Drug Administration 510(k) clearance of the CD Horizon Fenestrated Screw Set, which can be used for patients diagnosed with advanced stage tumors involving the thoracic and lumbar spine. This marks the first U.S. clearance for cement-augmented pedicle screws. The … Read More