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BioWorld - Tuesday, February 10, 2026
Home » Topics » Regions » Europe

Europe
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Medtronic scores CE marking for Bluesync-enabled implantable defibrillators

Jan. 31, 2020
By Meg Bryant
Medtronic plc has gained CE mark approval for its Cobalt and Crome portfolio, the company’s first implantable cardiac defibrillators (ICDs) and cardiac resynchronization therapy-defibrillators (CRT-Ds) to offer connected health via Bluesync technology. The portfolio will be rolled out on a country-by-country basis throughout Europe, with initial implants in select countries to begin soon.
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1-31-GE-Healthcare-Pristina-Serena.png

GE Healthcare performs first angiomammography-guided breast biopsy in France

Jan. 31, 2020
By Bernard Banga
PARIS – The European mammography division of GE Healthcare Inc., based in Buc, France, has just performed the first breast biopsy guided by angiomammography, using the Pristina Serena biopsy robot on a patient at the Gustave Roussy Institute in Villejuif, France.
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EU panel CHMPions varied batch of prospective new therapies

Jan. 31, 2020
By Randy Osborne
The EMA’s Committee for Medicinal Products for Human Use (CHMP) looked with favor on a bucketload of would-be drugs, issuing positive opinions for the European Commission to consider across a range of indications.
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EU greenlights Abbott’s transcatheter mitral valve replacement device

Jan. 30, 2020
By Meg Bryant
Abbott Laboratories has received CE mark approval for its Tendyne transcatheter mitral valve implantation (TMVI) system, the first such device approved for use in Europe and the world. The system is intended for patients with leaky mitral valves that are beyond repair and those at high risk for open heart surgery.
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Belgian flag and piggy bank

White Fund secures $22M to finance promising med-tech projects

Jan. 30, 2020
By Bernard Banga
PARIS – White Fund SA, of Lièges, Belgium, secured $22 million for early stage financing of Belgian med-tech companies. “Our shareholders are investing in a specialized fund [that], beyond financial returns, [creates] expectations in terms of supporting the strong med-tech ecosystem in Belgium and advantages in terms of job creation,” explained Benoît Fellin, investment manager at Noshaq SA, manager of the White Fund.
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Bag of euros

Sequana raises €19M for U.S. and European Alfapump trials

Jan. 28, 2020
By Nuala Moran
LONDON – Sequana Medical NV has raised €19 million (US$21 million) in a private placing to fund continuation of the U.S. pivotal trial of its Alfapump in treating ascites due to cirrhosis of the liver and a European trial of the device in heart failure patients who have stopped responding to diuretics.
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Owen Smith, professor of pediatric and adolescent medicine, University College Dublin
Genomics Summit 2020

Ireland’s embrace of genomics remains tentative

Jan. 23, 2020
By Cormac Sheridan
DUBLIN – “Welcome to the conversation,” Abbvie Inc.’s head of genomic research, Howard Jacob, an early pioneer of genomics-driven medicine, told delegates during a keynote address at the Genomics Summit 2020 event Jan. 23. Ireland is very much a latecomer to that conversation and it has yet, as a country, to figure out what the shape of its contribution to the genomic era of medicine is going to be.
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AI microchip illustration

French university hospitals grasp AI

Jan. 21, 2020
By Bernard Banga
PARIS – EY SAS has published the results of the first edition of a barometer dedicated to the role of artificial intelligence (AI) in French public hospitals. The health care sector, which is undergoing wholesale change in France, is suffering tight economic constraints and faces ever-increasing expectations from patients. “The development of [AI] in France is a priority. It's a matter of gauging it,” Loïc Chabanier, an EY partner responsible for health care, told BioWorld.
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Oviva raises $21M to advance diabetes treatment program in Europe

Jan. 17, 2020
By Nuala Moran
LONDON – Oviva AG has raised US$21 million in a series B funding to further advance commercialization of its digital diabetes treatment program across Europe.
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Map of Europe

EU posts guidelines for medical device cybersecurity

Jan. 15, 2020
By Nuala Moran
LONDON – The European Commission has published new guidelines on cybersecurity for medical devices, putting flesh on the bones of the requirements in the Medical Device Regulation (MDR) that comes into force in May.
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