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BioWorld - Friday, July 17, 2026
Home » Topics » Europe, Medical technology

Europe, Medical technology
Europe, Medical technology RSS Feed RSS

EU achieves first-ever bronchoscopy-guided microwave ablation of lung nodules

Jan. 5, 2023
By Bernard Banga
A surgical team from the Curie-Montsouris Chest Center in Paris, has successfully performed thermal ablation of a metastatic lung lesion using microwaves via a computer tomography (CT)-guided endobronchial approach.
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Bottneuro patient

Bottneuro secures $4.3M to develop its non-invasive Alzheimer’s treatment

Jan. 4, 2023
By Bernard Banga
Bottneuro AG closed the first tranche of a bridge round, bringing its total capital raise in 2022 to $4.3 million. This is being used to develop its noninvasive, domestic therapy for treating early moderate-stage Alzheimer’s patients.
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Clinical data illustration

MHRA advocates use of synthetic datasets in clinical trials

Jan. 3, 2023
By Nuala Moran
The U.K. Medicines and Healthcare products Agency (MHRA) reported a trio of research projects as part of a push to maintain its reputation as a leading regulator of drugs and medical devices now the U.K. is no longer part of EU regulatory systems, and to attract clinical trials - and the associated inward investment - despite no longer offering access to the EU single market.
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Numares gets $21.2M to develop a new MRS-based diagnostic platform

Dec. 29, 2022
By Bernard Banga
Numares Health AG received $21.2 million from the European Investment Bank (EIB) in support to its automated and software based IVD platform for obtaining high-quality nuclear magnetic resonance metabolomics data from blood or urine biopsy samples.
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Seekin’s cancer mutation detection kit receives CE-IVD mark

Dec. 27, 2022
By Zhang Mengying
Seekin Inc.’s cancer mutation detection kit Pancanseek for leukemia patients has received a CE-IVD mark, expanding the company’s reach in the testing space.
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Person holding Carmat's bio-prosthetic artificial heart

Carmat raises $33M to increase production of its bio-prosthetic artificial heart

Dec. 27, 2022
By Bernard Banga
Carmat SA just completed a flash fundraising of $33 million to increase production of its Aeson total artificial heart and support sales growth in Europe. The operation featured two distinct but concurrent actions: a reserved offer and a public offer. The reserved offer, intended for specialist investors, raised $28.9 million.
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European Union flag
’22 in review

EU’s Medical Device Regulation stumbles into 2023 on a collision course with reality

Dec. 22, 2022
By Mark McCarty
The European Union’s efforts to update its regulatory framework for medical devices was heralded as a long-overdue response to the Poly Implant Prothèse (PIP) breast implant scandal, but the COVID-19 pandemic added significant drag to the implementation timelines. Those timelines have proven impracticable for other reasons as well and the problem will bleed into the new year and perhaps beyond to the detriment of patients and manufacturers.
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Christophe Moser and Laura Kowalczuk with Cellularis

Cellularis device enables early diagnosis of degenerative eye disorders

Dec. 20, 2022
By Bernard Banga
Earlysight SA is developing a novel ophthalmology device that can be used to diagnose certain degenerative eye disorders long before onset of first symptoms. Earlysight and researchers at the Swiss Federal Institute of Technology Lausanne (EPFL) have reported positive results for their first clinical trial of Cellularis in the journal Ophthalmology Science.
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Newborn feet

UK newborn genome project targeting rare disease backed by £105M

Dec. 19, 2022
By Nuala Moran
The U.K. is taking the next step in applying genomics to health care with the launch of a £105 million (US$130 million) project that will sequence the whole genomes of 100,000 healthy newborn babies to detect rare genetic conditions.
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UK to decide whether to recognize FDA approvals of med tech

Dec. 19, 2022
By Nuala Moran
The U.K. is mulling over whether to recognize U.S. FDA approvals of medical devices as part of moves to accelerate the implementation of its post-Brexit regulatory system.
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