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BioWorld - Sunday, July 26, 2026
Home » Topics » Europe, BioWorld

Europe, BioWorld
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European Commission headquarters

European Commission floats broad framework for regulation of artificial intelligence

May 6, 2021
By Mark McCarty
The European Commission posted a draft legislative framework for regulation of artificial intelligence, a document that spans all potential uses of such algorithms rather than just medical ones.
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Pfizer-Biontech COVID-19 vaccine vial

Single dose of Pfizer vaccine not strong enough against variants, U.K. study shows

May 3, 2021
By Nuala Moran
LONDON – A single dose of Pfizer Inc./Biontech SE’s COVID-19 vaccine does not promote a strong enough immune response to provide protection against variants of SARS-CoV-2, including the Kent variant B.1.1.7, which as of April 29 had caused 226,635 confirmed infections in the U.K.
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Biotech first: EC fines company over M&A divestiture info

May 3, 2021
By Mari Serebrov
In a first for the biotech industry, the European Commission (EC) has imposed a €7.5 million (US$9.05 million) fine on Sigma-Aldrich, under the EU’s 2004 Merger Regulation, for providing incorrect or misleading information during a merger investigation.
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Patient in hospital bed

Real-world U.K. data show small number of COVID-19 vaccine failures

April 30, 2021
By Nuala Moran
LONDON – The latest tranche of data from an array of large-scale COVID-19 studies running in the U.K. provides real-world evidence that vaccines have a dramatic effect in preventing hospitalization and death, but that there are a very small number of vaccine failures. The data cover 3,842 people who received a vaccine and subsequently were admitted to the hospital between Dec. 8, 2020, when the national vaccination rollout began, and the data cutoff of April 10, 2021.
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Box of Astrazeneca COVID-19 vaccine vials

EC to take Astrazeneca to court over vaccine supply

April 27, 2021
By Mari Serebrov
Astrazeneca plc’s saga of its COVID-19 vaccine continued this week with the European Commission (EC) deciding to begin legal action against the Cambridge, U.K.-based company, claiming it has failed to deliver doses in line with its contract.
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EMA icons

EMA review supports continued use of Astrazeneca vaccine in all adults

April 23, 2021
By Cormac Sheridan
DUBLIN – The European Medicines Agency (EMA) has reiterated its support for Astrazeneca plc’s Vaxzervia COVID-19 vaccine, following an interim analysis of a data review, which the agency’s Committee on Human Medicinal Products (CHMP) has conducted over the past two weeks.
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Drug vial and syringe

Single dose of Astrazeneca or Pfizer/Biontech COVID-19 vaccine cuts infections by 65%

April 23, 2021
By Nuala Moran
LONDON – A large scale U.K. study looking at the impact of COVID-19 vaccinations on antibody responses and new infections in 373,402 people in the general population has shown a single dose of vaccine cut infections by 65%. Symptomatic infections fell by 74% and infections with no reported symptoms by 57%, 21 days after receiving the first dose of either Astrazeneca plc’s or Pfizer Inc./Biontech SE’s vaccine.
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Coin stacks, dollar signs and up arrow

Business as usual: Versant raises $950M for three new funds

April 21, 2021
By Cormac Sheridan
Versant Ventures has closed three new funds with an aggregate raise of $950 million to allocate to the next wave of innovative startups across North America and Europe. The money is new, but everything else is more or less unchanged. “It’s the same strategy, same team, same geography, same operational model,” Versant chairman and managing director Brad Bolzon told BioWorld.
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Capsule with Swiss flag

Swiss biotech shrugs off COVID-19 woes as investment reaches new heights in 2020

April 20, 2021
By Cormac Sheridan
DUBLIN – In keeping with the record-breaking year for biotech fundraising across the globe, the Swiss biotech sector also scaled new heights in 2020, with aggregate investment of CHF3.4 billion (US$3.7 billion), according to the newly published Swiss Biotech Report 2021. It represents almost a threefold increase on the CHF1.2 billion total it logged in 2019.
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EMA calls for warning to label but says J&J COVID-19 vaccine benefit outweighs risk

April 20, 2021
By Nuala Moran
LONDON – The EMA’s safety committee has concluded that unusual blood clots with low blood platelets are a rare side effect of Johnson & Johnson Inc.’s COVID-19 vaccine and that a warning should be added to the label. The decision is based on all available evidence, which currently consists of eight reports from the U.S. of serious cases of thrombosis, one of which was fatal. All cases were in people under 60 years of age, and within three weeks after vaccination, the majority in women. One case occurred during the clinical trials. 
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