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BioWorld - Thursday, February 19, 2026
Home » Topics » Regions » Europe

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Female doctor and patient
FT Global Pharma and Biotech Summit

Could restricting diversity efforts stall women’s health research?

Nov. 12, 2025
By Nuala Moran
No Comments
Recent progress in redressing the historical underfunding and neglect of women’s health could be undermined by the backlash against diversity, equity and inclusion (DEI) initiatives, according to executives participating in the FT Global Pharma and Biotech Summit 2025 in London Nov. 11-12.
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Illustration showing cross-section of bladder with tumor on bladder wall

Minze, Medtronic partner on overactive bladder care in EMEA

Nov. 12, 2025
By Shani Alexander
Minze Health NV signed a three-year agreement with Medtronic plc to bring its Minze Diary Pod, an app-controlled automated urine collection device, to markets across the EMEA region. The partnership aims to enhance the support services available for patients with overactive bladder receiving sacral neuromodulation therapy with Medtronic’s Interstim system.
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Europe map, white on blue

MDCG announces pilot for coordination of EU clinical trials

Nov. 12, 2025
By Mark McCarty
One of the problems of doing business in the EU is that each member nation has its own more or less unique requirements for clinical trial registration, but the Medical Device Coordination Group may have a solution in the form of a pilot program for harmonized clinical trial registration.
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Pill with Euro currency symbol
FT Global Pharma and Biotech Summit

Trump’s MFN price deals a wake-up call for governments in Europe

Nov. 11, 2025
By Nuala Moran
No Comments
The industry has been complaining about the drug pricing and reimbursement policies of European governments for years, but only now with the Trump administration’s moves to enforce most favored nation (MFN) pricing and reduce the U.S./EU price gap are governments facing up to the reality that they will have to pay more for new drugs.
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SPT Labtech Firefly

SPT Labtech expands partnerships to boost firefly platform

Nov. 11, 2025
By Shani Alexander
SPT Labtech Ltd. recently partnered with Alithea Genomics SA to integrate its firefly liquid handling platform with Alithea’s single-cell RNA-sequency technology to create a scalable and reproducible workflow for transcriptomics research.
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International currency symbols
Med-tech financings October 2025

Med-tech financings reach $26.6B as sector recovery continues

Nov. 11, 2025
By Amanda Lanier
Med-tech financings with disclosed valuations from January through October 2025 totaled $26.58 billion, nearly matching 2022’s $26.83 billion and marking a continued recovery from the sector’s 2023 low of $15.59 billion. The data suggest renewed investor confidence in med-tech, with capital flows shifting back toward public markets after two years of restrained activity.
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Pfizer Inc. signage

Pfizer, Metsera reach $10B merger agreement as Novo bows out

Nov. 10, 2025
By Jennifer Boggs
No Comments
Pfizer Inc. emerged over the weekend as the winner of the bidding war for Metsera Inc., with the two reaching an amended agreement after market close Nov. 7 that values the obesity drugmaker at about $10 billion. The next day, the other contender, Novo Nordisk A/S, confirmed it does not intend to increase its most recent offer.
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Heartflow FFRCT analysis Credit: Heartflow Inc.
AHA Scientific Sessions

FISH&CHIPS serves up appetizing news for Heartflow

Nov. 10, 2025
By Mark McCarty
Shares of Mountain View, Calif.-based Heartflow Inc. have oscillated significantly over the past three months, but the results of a study of the company’s plaque staging system have breathed new life into the company’s shares, boosting them by 7% in Nov. 10 trading.
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Symani system

MMI gets IDE for robotic microsurgical study in Alzheimer’s

Nov. 10, 2025
By Holland Johnson
Medical Microinstruments Inc., reported the U.S. FDA approval of an investigational device exemption for a study using its Symani surgical system for treating Alzheimer’s disease, one of its earliest forays into the brain.
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British flag

UK’s MHRA eyes rare disease framework for therapeutic products

Nov. 7, 2025
By Mark McCarty
The U.K. Medicines and Healthcare Products Regulatory Agency has laid out an approach to medical products for rare diseases, which the agency said afflict 3.5 million U.K. citizens. One of the objectives of this program is to simplify evidence requirements for these therapies with the hope of providing patients with more rapid access to much-needed therapeutic options.
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