COMMUNIQUÉS West-GlobeNewswire

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Oxford Biomedica completes acquisition of ABL Europe
29/01/2024 -
Applied UV Inc. Announces Receipt of Provisional Patent for Our Pulse Modulated UVC LED System to be Added to Our Patented Fighter Flex LED Solution Expanding Significant Revenue Opportunity
29/01/2024 -
Fortrea Announces Date for Fourth Quarter and Full Year 2023 Financial Results and Conference Call
29/01/2024 -
ANI Pharmaceuticals to Participate at the Guggenheim Healthcare Talks | 6th Annual Biotechnology Conference
29/01/2024 -
21e Guignolée Dr Julien : Montant historique de 4,2 M$ pour les enfants en situation de vulnérabilité
29/01/2024 -
Werth Family Investment Associates Converts Remaining $3.3M of Debt and Accrued Interest into Cingulate Equity at Premium to Market
29/01/2024 -
Oculis to Present at Upcoming February Investor Conferences
29/01/2024 -
KFSH&RC-Madinah Receives Prestigious 2023 Press Ganey Human Experience Guardian of Excellence Award
29/01/2024 -
Vera Therapeutics Announces Proposed Public Offering of Class A Common Stock
29/01/2024 -
Panbela Announces Pricing of Approximately $9.0 Million Public Offering
29/01/2024 -
Gamida Cell Actively Pursuing Strategic Alternatives
29/01/2024 -
The combination of Novozymes and Chr. Hansen is now successfully completed, creating Novonesis – a leading global biosolutions partner
29/01/2024 -
Completion of the combination between Novozymes and Chr. Hansen
29/01/2024 -
Completion of the combination between Novozymes and Chr. Hansen
29/01/2024 -
Alvotech Announces Positive Top-Line Results from a Pharmacokinetic Study for AVT03, a Proposed Biosimilar for Prolia® and Xgeva®
29/01/2024 -
Orion Corporation and Newel Health enter into licensing agreement for a digital therapeutic (DTx) ODD-403 (“Rohkea”) in pain
29/01/2024 -
Alvotech Announces Positive Top-Line Results from a Pharmacokinetic Study for AVT03, a Proposed Biosimilar for Prolia® and Xgeva®
29/01/2024 -
Vidac Pharma reports positive interim Phase 2a data in orphan disease cutaneous T-cell lymphoma (CTCL) with lead asset VDA-1102
29/01/2024 -
Vidac Pharma annonce des données positives de l'analyse intermédiaire de phase 2a pour son produit phare VDA-1102 dans le traitement des Lymphomes T cutanés (LCT), une maladie rare.
29/01/2024
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