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INOVIO Reports FDA Partial Clinical Hold for Planned Phase 2 / 3 Trial of COVID-19 Vaccine Candidate INO-4800

INOVIO, a biotechnology company focused on bringing to market precisely designed DNA medicines to treat and protect people from infectious diseases and cancer, announced that the U.S. FDA has notified the company it has additional questions about the company's...

Centus Biotherapeutics Receives European Marketing Authorization for Equidacent, Biosimilar Avastin

Centus Biotherapeutics Ltd., a joint venture between Fujifilm Kyowa Kirin Biologics Co., Ltd. and AstraZeneca, announced that the European Commission (EC) has granted the marketing authorization for Equidacentยฎ (Product Code: FKB238), the company's biosimilar to Avastinยฎ (bevacizumab). The authorization follows...

Genetron, CStone start clinical trial in China to develop CDx for avapritinib

Genetron and its partner CStone Pharmaceuticals have commenced a clinical trial in China, to jointly develop a companion diagnostic (CDx) test for avapritinib. Discovered by Blueprint Medicines, Avapritinib is a US Food and Drug Administration (FDA) approved kinase inhibitor, to...

High Purity New England Supports Drug Development Pipelines with Fully Customizable and Flexible Single-Use Assembly Solution

Demand for single-use assembly solutions in the biopharma industry continues to increase, with the market expected to be worth $26.89 billion by 2025. To help meet that demand, High Purity New England (HPNE), a leading supplier of biopharma equipment and...

Sterling Pharma Solutions acquires API facility in the US

Global contract development and manufacturing organisation (CDMO), Sterling Pharma Solutions, has announced its acquisition of Alcamiโ€™s Germantown, Wisconsin facility in the US. The new facility will further bolster Sterlingโ€™s US presence and will provide additional capacity for customer API development...

BD Announces CE Mark of Portable, Rapid Point-of-Care Antigen Test to Detect SARS-CoV-2 in 15 minutes

BD (Becton, Dickinson and Company), a leading global medical technology company, announced its rapid, point-of-care, SARS-CoV-2 antigen test for use on the BD Veritorโ„ข Plus System has been CE marked to the IVD Directive (98/79/EC). BD has announced CE Mark...

Regenerative Medicine Market Rapidly Growing Worldwide at Healthy CAGR

As per the Organ Procurement and Transplantation Network, 36,527 organ transplants were accomplished in the United States in 2020. Regenerative medicines plays a vital role in transplants as it refers to an interdisciplinary field and is a branch of...

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