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(GlobeNewswire) - ProLynx Inc., a biotech company with a unique technology for tunable half-life extension of drugs, announced publication of a paper entitled Could a Long-Acting Prodrug of SN-38 be [...]

The European Commission recently approved the plan of the Interreg program supporting cross-border developments, so applications can start from the beginning of next year, Minister of Foreign Affairs and Trade [...]

Scope of Work: Construction of 200-MW electrolysis plant in Normandy. Description: The distribution of the state funds will hinge on the approval from the European Commission. The 200-MW electrolyser will [...]

Harbour BioMed ('HBM', HKEX: 02142) announced that the China National Medical Products Administration (NMPA) has approved its Investigational New Drug (IND) applications for HBM4003, a next-generation, fully human anti-CTLA-4 monoclonal [...]

The Ministry of Economy and Innovation intends to receive 40 million from the Ministry of Environment, which administers the Modernization Fund established by the European Union, by the end of [...]

Indias drug regulatory authority is likely to take up Zydus Cadila's application seeking Emergency Use Authorisation (EUA) for its Covid-19 vaccine this week. If it gets approval, it will be [...]

Hyderabad-based Bharat Biotech today said that the USFDA had earlier communicated that no new Emergency Use Authorisation (EUA) will be approved for covid vaccines, a day after its US partner [...]

RheaVita, a company pioneering continuous freeze-drying technology for biopharmaceutical products, announced today that the company has closed a EUR 2.5 million Series A Financing. The round was co-led by Novalis [...]

Applications Based on Progression-Free Survival, Overall Survival, and Objective Response Rate Data From Respective Pivotal Phase 3 Trials Merck, known as MSD outside the United States and Canada, and Eisai [...]

AbbVie (NYSE: ABBV) today announced that it has submitted applications to the U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA) seeking approval for RINVOQ (upadacitinib) for the [...]

Micron Biomedical, Inc. (Micron) recently received a second tranche of funding ($2.6M) to continue clinical development of its microneedle-based technology for measles and rubella vaccination from the Bill & Melinda [...]

AMERI Holdings, Inc. (NASDAQ: AMRH) ('Ameri'), announced that its proposed amalgamation partner Jay Pharma Inc. ('Jay Pharma' or 'the Company') has announced the addition of new senior staff as the [...]

Roche has received approval from the US Food and Drug Administration (FDA) for Phesgo, in combination with intravenous (IV) chemotherapy, to treat early and metastatic human epidermal growth factor receptor [...]

Royal Philips (NYSE:PHG) announced today that FDA has granted premarket approval for the companys HeartStart FR3 and HeartStart FRx automated external defibrillators. The HeartStart FR3 is a professional-grade AED. It [...]

(GlobeNewswire) - June 23, 2020 Amsterdam, the Netherlands and Cambridge, MA Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that the Center for Devices [...]

(GlobeNewswire) - June 23, 2020 Amsterdam, the Netherlands and Cambridge, MA Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that the Center for Devices [...]

Aladdin Healthcare Technologies SE ('Aladdin', ISIN: DE000A12ULL2), a leading developer of Artificial Intelligence (AI) based healthcare diagnostics and drug discovery applications, gained approval by the Dementias Platform UK (DPUK) for [...]

The Janssen Pharmaceutical Companies of Johnson & Johnson announced the submission of two supplemental Biologics License Applications (sBLA) to the U.S. Food and Drug Administration (FDA) seeking approval of SIMPONI [...]

The Janssen Pharmaceutical Companies of Johnson & Johnson today announced the submission of two supplemental Biologics License Applications (sBLA) to the U.S. Food and Drug Administration (FDA) seeking approval of [...]

Merck, known as MSD outside the United States and Canada, announced that the U.S. Food and Drug Administration (FDA) has accepted for review six supplemental Biologics License Applications (sBLAs) to [...]

xinhuanet.com The Acuvue Oasys Contact Lenses with Transitions Light Intelligent Technology are soft contact lenses indicated for daily use to correct the vision of people with non-diseased eyes who are [...]

(GlobeNewswire) - Advanced Accelerator Applications S.A. (NASDAQ:AAAP) (AAA or the Company), a Novartis company and leader in nuclear medicine theragnostics, today announced that it has received US Food and Drug [...]

A major provider of automated, multiplex molecular diagnostic testing systems, GenMark Diagnostics, Inc., has filed 510(k) applications for its ePlex sample-to-answer instrument and Respiratory Pathogen Panel, with the FDA. In [...]

Janssen Biotech, Inc. (Janssen) announced today the submission of two Supplemental Biologics License Applications (sBLAs) to the U.S. Food and Drug Administration (FDA) seeking approval of SIMPONI ARIA (golimumab) for [...]

Biogen today announced that its New Drug Application (NDA) for nusinersen, an investigational treatment for spinal muscular atrophy (SMA), has been accepted by the U.S. Food and Drug Administration (FDA) [...]

Backed by Scottish Enterprise's Scottish Investment Bank, a pharmaceuticals company, is preparing for a second-stage clinical test of a superbug-resistant drug after it was designated a Qualified Infectious Disease Product [...]

The European Commission has approved the Italian support scheme for renewable energies, concluding that the scheme was in line with EU state aid rules and that it would further EU [...]