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BioWorld - Monday, July 6, 2026
Home » Topics » Regions » Europe

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Total artificial heart being manufactured

Carmat's artificial heart receives CE mark

Dec. 23, 2020
By Annette Boyle
Carmat SA said its total artificial heart received the CE mark, and the company plans to ramp up production to enable the launch of the device in the second quarter of 2021. The artificial heart offers a bridge to transplant in patients with end-stage biventricular heart failure. It provides an alternative for individuals for whom maximal medical therapy and left ventricular assist device are insufficient or contraindicated.
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Earth infected with pandemic

Equal access: 190 countries pool purchasing power for COVID-19 vaccines

Dec. 22, 2020
By Nuala Moran
LONDON – The COVAX initiative, set up in a bid to ensure equitable distribution of COVID-19 vaccines, is poised for a global rollout starting in Q1 2021, after sealing agreements to access 2 billion doses of a number of different products. That puts the world on a clear pathway to ending the acute phase of the pandemic, by protecting the most vulnerable people around the world, according to GAVI, the vaccines alliance, which is spearheading COVAX.
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Novai’s test gives early warning of onset of wet AMD

Dec. 22, 2020
By Nuala Moran
LONDON – Researchers at University College London (UCL) have devised a new eye test they say can predict the likelihood of developing wet age-related macular degeneration (AMD) up to three years before overt symptoms develop. The prognostic test involves injecting a fluorescent dye, via the arm, to tag stressed endothelial cells in the retina.
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European Union map and coronavirus

EMA authorizes Pfizer/Biontech vaccine as new SARS-CoV-2 variant emerges

Dec. 21, 2020
By Nuala Moran
LONDON – The EMA has issued a positive opinion on Pfizer Inc./Biontech SE’s COVID-19 vaccine, BNT-162b2, becoming the first regulator to recommend a full marketing authorization, rather than approval for emergency use. The vaccine, now brand named Comirnaty, still has to go through the formality of being approved by EU member state governments, but the EU health commissioner, Stella Kyriakides, has said she expects roll out to start on Dec. 27.
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Person using Odysight app on Ipad

Tilak partners with Novartis to expand its digital solution for vision monitoring

Dec. 21, 2020
By Bernard Banga
PARIS – Tilak Healthcare SAS is signing an ophthalmology partnership agreement with Novartis AG from Basel, Switzerland, to expand international distribution of its vision monitoring technology, Odysight.
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Earth infected with pandemic

Equal access: 190 countries pool purchasing power for COVID-19 vaccines

Dec. 18, 2020
By Nuala Moran
LONDON – The COVAX initiative, set up in a bid to ensure equitable distribution of COVID-19 vaccines, is poised for a global rollout starting in Q1 2021, after sealing agreements to access 2 billion doses of a number of different products. That puts the world on a clear pathway to ending the acute phase of the pandemic, by protecting the most vulnerable people around the world, according to GAVI, the vaccines alliance, which is spearheading COVAX.
Read More
Doctor viewing Brainquant software on computer

Braintale secures $1.2M seed round to boost commercialization of its brain injury assessment platform in Europe

Dec. 15, 2020
By Bernard Banga
PARIS – Braintale SAS has completed a $1.2 million seed round towards its portfolio of digital quantification and prediction medical devices for neurology and intensive care. This funding round, including a loan from Bpifrance, attracted investment from business angels, as well as industry and health care professionals.
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Biontech vaccine

EMA accelerates assessment of Pfizer-Biontech COVID-19 vaccine

Dec. 15, 2020
By Cormac Sheridan
DUBLIN – Bowing to public and political pressure, the EMA has brought forward its review of BNT-162b2, the mRNA-based COVID-19 vaccine jointly developed by Pfizer Inc. and Biontech SE, to Dec. 21, more than a week ahead of its originally scheduled date of Dec. 29.
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Benjamin Bertrand in the lab
Aortic stenosis solutions

Cardiawave on the way to CE mark for its pulsed cavitational ultrasound therapy

Dec. 14, 2020
By Bernard Banga
PARIS – Cardiawave SAS has been granted authorization by the French National Agency for Medicines and Health Products Safety to extend its clinical trial in France and treat patients with calcific aortic stenosis (AS).
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EMA’s CHMP delivers eight positive opinions in December, 61 for 2020

Dec. 11, 2020
By Cormac Sheridan
DUBLIN – The European Medicines Agency’s human medicines committee, the CHMP, all but closed out the year by issuing positive opinions on eight marketing authorization applications during its December meeting. Its work for 2020 is not quite yet done, however. It has scheduled an extraordinary meeting for Dec. 29 to review an application from Pfizer Inc. and Biontech AG for their mRNA COVID-19 vaccine BNT162b2.
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