Cosmos Health Releases 2026–2029 Guidance: Targeting $200M Revenue, $71M Gross Profit, and $44M Adjusted EBITDA by 2029 — Building an Innovative, High-Margin Healthcare Platform with Strong Cash Generation

May 26, 2026 09:34 ET  | Source: Cosmos Health Inc. CHICAGO, May 26, 2026 (GLOBE NEWSWIRE) — Cosmos Health Inc. (“Cosmos Health” or the “Company”) (NASDAQ:COSM), a diversified, vertically integrated global healthcare group, today announced its financial guidance for the 2026–2029 period. Cosmos Health enters this guidance period following its strongest financial performance in Company history — full year 2025 […]

AGC Biologics to Manufacture Teikoku Seiyaku’s rhMMP-7 Drug Substance

AGC Biologics to provide process development and GMP manufacturing for a novel therapy, leveraging its global microbial network across Germany and Japan. May 25, 2026 20:00 ET  | Source: AGC Biologics, Inc. HEIDELBERG, Germany and CHIBA, Japan, May 26, 2026 (GLOBE NEWSWIRE) — AGC Biologics, your friendly CDMO expert, was selected by Teikoku Seiyaku Co., Ltd., a

The hidden impact of veterinary care: new insights from a global survey of veterinarians

May 25, 2026 03:00 ET  | Source: Boehringer Ingelheim Limited Boehringer Ingelheim today published new global survey findings revealing the often-overlooked aspects of veterinary care that are essential in protecting animals, people, and society.  Drawing on responses from 1,046 qualifying veterinary professionals across 51 countries, the survey identified three of the most important yet underrecognized aspects of

CHMP issues positive opinion for JASCAYD® (nerandomilast), bringing a new IPF and PPF therapy closer to patients in the EU

May 22, 2026 08:15 ET  | Source: Boehringer Ingelheim Limited Not intended for US and UK media Ingelheim, Germany – Boehringer Ingelheim’s JASCAYD® (nerandomilast) has been recommended for marketing authorization by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency for the treatment of adults with idiopathic pulmonary fibrosis (IPF) and adults with progressive

China approves HERNEXEOS® as first targeted oral treatment option for HER2-mutant advanced NSCLC at initial diagnosis

May 22, 2026 03:45 ET  | Source: Boehringer Ingelheim Limited Not intended for UK and US media Ingelheim, Germany –Boehringer Ingelheim’s HERNEXEOS® (zongertinib tablets) has been conditionally approved as monotherapy by China’s National Medical Products Administration (NMPA) as an initial treatment for adult patients with unresectable, locally advanced or metastatic non-small cell lung cancer (NSCLC) whose tumors have activating

Together for Steatotic Liver Disease – The Hidden NCDs: SLD as the Next Global Public Health Priority

May 22, 2026 03:00 ET  | Source: Global Liver Institute Geneva, Switzerland, May 22, 2026 (GLOBE NEWSWIRE) — Yesterday, Global Liver Institute (GLI), in collaboration with the Egyptian Ministry of Health and Population, convened a high-level policy event, on the sidelines of the Seventy-Ninth World Health Assembly (WHA79) to translate this global policy milestone into coordinated action. The event,

Boehringer Ingelheim’s oncology portfolio shows strong promise across multiple cancers at ASCO 2026

May 21, 2026 17:00 ET  | Source: Boehringer Ingelheim Limited Not intended for US and UK media Ingelheim, Germany and Ridgefield, Conn., US –At the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting, Boehringer Ingelheim will present new data from across its robust oncology clinical development program. Key data includes patient-reported outcomes with HERNEXEOS® (zongertinib tablets) as an initial orally administered treatment option for HER2 (ERBB2)-mutant advanced

The European Medicines Agency Accepts Teva’s Marketing Authorization Application for Olanzapine Long-Acting Injectable (TEV-‘749) for the Treatment of Schizophrenia in Adults

May 21, 2026 12:30 ET  | Source: Teva Pharmaceutical Industries Ltd TEL AVIV, Israel and PARIS, May 21, 2026 (GLOBE NEWSWIRE) — Teva Pharmaceuticals International GmbH, a subsidiary of Teva Pharmaceutical Industries Ltd. (NYSE: and TASE: TEVA) and Medincell (Euronext: MEDCL), today announced that the European Medicines Agency (EMA) has accepted the Marketing Authorization Application (MAA) for

Junshi Biosciences Announces Approval of Toripalimab NDA for the 1st-line treatment of HER2 Expressing Urothelial Carcinoma

May 21, 2026 06:28 ET  | Source: Junshi Biosciences SHANGHAI, May 21, 2026 (GLOBE NEWSWIRE) — Shanghai Junshi Biosciences Co., Ltd (Junshi Biosciences, HKEX: 1877; SSE: 688180), a leading innovation-driven biopharmaceutical company dedicated to the discovery, development, and commercialization of novel therapies, announced that the new drug application (NDA) for toripalimab in combination with disitamab vedotin for

Hanmi Pharmaceutical Partners with Organon to Export Combination Therapies to Southeast Asia

Cardiovascular and Respiratory medicines to be supplied in Malaysia and the Philippines May 21, 2026 05:06 ET  | Source: Hanmi Pharmaceutical Shin Hae-gon (right), Head of Overseas Sales at Hanmi Pharmaceutical, and Andreas Daugaard Jørgensen (left), Managing Director, Organon Asia Pacific Cluster, met at Organon’s Malaysia office to discuss the expansion of Hanmi’s combination therapies into the

Curia Completes Upgrade of API Aseptic Suites in Valladolid, Spain

May 19, 2026 09:00 ET  | Source: Curia Global, Inc. ALBANY, N.Y., May 19, 2026 (GLOBE NEWSWIRE) — Curia Global, Inc. (Curia), a leading global research, development and manufacturing organization, today announced the completion of its upgrade to its two aseptic suites in Valladolid, Spain. The $4 million dollar investment is in accordance with the EU’s GMP

Risen Pharma Announces Initiation of Phase 2 Clinical Trial of RP902 for Mild Cognitive Impairment Due to Alzheimer’s Disease

May 19, 2026 08:24 ET  | Source: Risen Pharma Tech Co., Ltd SHANGHAI, May 19, 2026 (GLOBE NEWSWIRE) — Risen Pharma, a clinical-stage biotech company focusing on the development and commercialization of high-need, patient-accessible therapeutics, today announced the initiation of a Phase 2 clinical study in China of RP902, an oral small-molecule drug developed to address significant unmet

Philips highlights advances in imaging and physiology to support complex PCI at EuroPCR 2026

May 18, 2026 11:00 ET  | Source: Royal Philips May 18, 2026 From imaging to AI-enabled guidance, Philips connects technologies into a unified workflow to improve efficiency, reduce radiation exposure and support procedural confidenceAmsterdam, the Netherlands – As cardiac procedures become more complex, interventional cardiologists must balance the need for precise imaging and decision-making with growing pressure to

Philips introduces SmartIQ to address the trade-off between image quality and radiation dose in coronary procedures

May 18, 2026 10:00 ET  | Source: Royal Philips May 18, 2026      Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced Philips SmartIQ, a breakthrough coronary imaging technology for its Azurion image-guided therapy. Developed in collaboration with leading cardiovascular centers, SmartIQ is designed to address one of the field’s most

Fitch Upgrades Teva to Investment Grade Amid Pivot to Growth Execution

May 18, 2026 08:30 ET  | Source: Teva Pharmaceutical Industries Ltd TEL AVIV, Israel, May 18, 2026 (GLOBE NEWSWIRE) — Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced that Fitch Ratings Agency (“Fitch”) has raised the Company’s corporate credit rating to Investment Grade BBB-, with a stable outlook, from BB+. “This strong endorsement, our third

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