Pharma Press Releases

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Celltrion Expands Biosimilar Portfolio in the European Union Following European Commission Approval of Two Biosimilars

Wednesday, February 19, 2025

Celltrion today announced that the European Commission EC has granted marketing authorization for three products across two biosimilars Eydenzelt CTP aflibercept a biosimilar to Eylea to treat multiple retinal disorders including neovascular wet ager...

Nomination period opens for IHF Awards and i-to-i Innovation Hub 2025

Wednesday, February 19, 2025

The International Hospital Federations Awards the premier annual awards programme for hospitals and healthcare organizations worldwide will celebrate years of rewarding excellence in healthcare leadership at the edition

CDMO Live Debuts as BioPharma Manufacturing Sector Approaches $200 Billion

Tuesday, February 18, 2025

CDMO Live has emerged as the definitive industry gathering bringing together Europes leading pharmaceutical outsourcing decisionmakers at Rotterdams World Trade Center this May putting the spotlight on this critical sector

TAHO Pharmaceuticals Reports Positive Results from Pivotal Study of TAH3311, the First Oral Dissolving Film Anticoagulant

Tuesday, February 18, 2025

TAHO Pharmaceuticals announces positive preliminary results from the pivotal study of TAH the worlds first Apixaban oral dissolving film ODF The study confirmed that TAH is bioequivalent to US and European reference Apixaban tablets

Baltics leading pharmaceutical company Grindeks expands to new export markets worldwide

Tuesday, February 18, 2025

The leading pharmaceutical company in the Baltics Grindeks continues to strengthen its global presence by entering new export markets This year for the first time Grindeks products will be delivered to Panama The companys export markets already inclu...

Rznomics Inc. Liver Cancer Drug Candidate Secures Fast Track Designation

Tuesday, February 18, 2025

Rznomics announced on the th that its anticancer drug RZ has received Fast Track Designation from the US Food and Drug Administration FDA for the treatment of Hepatocellular Carcinoma HCC

Fosun Pharma Deeply Embraces AI, Self-developed PharmAID Decision Intelligence Platform Boosts Efficient Innovation

Monday, February 17, 2025

Nowadays artificial intelligence AI technology is profoundly reshaping the landscape of the pharmaceutical and healthcare industry As a global innovationdriven pharmaceutical and healthcare group Fosun Pharma places great emphasis on the transformati...

Samsung Bioepis Gains European Commission (EC) Approval for Denosumab Biosimilar (OBODENCE™, XBRYK™)

Monday, February 17, 2025

Samsung Bioepis Co Ltd today announced that the European Commission EC has granted marketing authorization for OBODENCE mg prefilled syringe and XBRYK mg vial denosumab biosimilars referencing Prolia and Xgeva formerly referred to as SB

U.S. FDA Grants Full Approval of Deciphera’s ROMVIMZA™ (vimseltinib) for the Treatment of Symptomatic Tenosynovial Giant Cell Tumor (TGCT)

Saturday, February 15, 2025

Ono Pharmaceutical Co Ltd announced that the US Food and Drug Administration FDA has approved ROMVIMZA vimseltinib a kinase inhibitor for adult patients with symptomatic tenosynovial giant cell tumor TGCT for which surgical resection will potentially...

Kexing Biopharm Obtained IND Approval for Its Self-developed GB05 from U.S. FDA

Saturday, February 15, 2025

Kexing Biopharm Co Ltdrecently announced that the Investigational New Drug Application IND of GB Human Interferon b Inhalation Solution a selfdeveloped product by the Companys whollyowned subsidiary Shenzhen Kexing Pharmaceutical Co Ltd