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BioWorld - Thursday, January 22, 2026
Home » Topics » Regions » Europe

Europe
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EIB backs €72M round to advance Minervax’s group B step vaccine

Dec. 15, 2022
By Nuala Moran
Minervax Aps has closed a €72 million (US$76.6 million) financing round, enabling it to accelerate phase II development of its group B streptococcus (GBS) vaccine for the prevention of stillbirth and serious infections in newborns and complete the program next year.
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Newborn feet

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

Dec. 14, 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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EC to extend MDR-IVDR deadlines in face of mounting concerns

Dec. 13, 2022
By Nuala Moran
The European Commission has given in to the increasing pressure and alarm from member states and is moving to extend the deadlines for implementing the 2017 Medical Device Regulation (MDR) and the In Vitro Devices Regulation (IVDR).
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Natus buys Micromed to expand footprint with neurodiagnostic and neuromonitoring devices

Dec. 12, 2022
By Bernard Banga
Natus Medical Inc. entered into a definitive agreement to acquire EU-based neurophysiology solution provider Micromed Group SpA. The transaction is expected to close in early 2023, subject to regulatory approvals from the Italian Council of Ministers’ Presidency and the French Ministry of Economy and Finance. Full terms of the transaction have not been disclosed. “The idea behind this acquisition is to provide a single portfolio of neurodiagnostic and neuromonitoring products in the EU and the whole world,” Thomas Sullivan, CEO of Natus Medical, told BioWorld.
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Mainstay

Neurostimulation device for lower back pain gets boost from two back-to-back clinical trials

Dec. 9, 2022
By David Godkin
Mainstay Medical Holdings plc released data from a one-year, real-world, study of patients implanted with a neurostimulation device to treat chronic lower back pain.
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Switzerland set to import more US med tech in face of unfavorable EU market rules

Dec. 5, 2022
By Nuala Moran
Switzerland is making moves to allow the import of U.S. FDA-approved medical devices after losing barrier-free access to the EU market and over rising concerns about the dismal pace of implementation of the EU’s upgraded devices regulations.
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Uromems

Uromems initiates first-in-human study of its smart implant for treating SUI

Dec. 2, 2022
By David Godkin
Uromems SAS reported the successful completion of the first-in-human implant of a smart, automated artificial urinary sphincter (AUS) device for treating stress urinary incontinence (SUI). This initial pilot study recently saw the first male patient implanted with the Uroactive System at Paris’s La Pitié-Salpêtrière University Hospital and is considered by the company to be a key milestone in the technology’s development.
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New joint venture developing electron Flash therapy platform for treating cancer

Dec. 1, 2022
By Bernard Banga
Vaudois University Hospital (CHUV), in conjunction with the European laboratory for particle physics (CERN) and Theryq SAS, has signed an agreement to develop equipment for a novel radiotherapy technique known as “electron Flash therapy.” The new device will use very high energy electron (VHEE) radiation to treat cancers resistant to conventional therapy.
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European Union flag

EU states working around MDR issues, but the scope of solutions remains fragmented

Nov. 30, 2022
By Mark McCarty
A variety of governmental entities in the EU are feeling pressure to address the issues with the rollout of the Medical Device Regulation, and some EU member states have taken matters into their own hands.
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SurgiField

Surgibox wins CE mark, humanitarian use nod for OR in a backpack

Nov. 30, 2022
By Meg Bryant
Surgibox Inc. won a CE mark for two components of its Surgifield system, an ultraportable sterile system that enables safe surgery any place, any time. The five-year-old startup also landed a humanitarian use exemption for use of the system in war-torn Ukraine.
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