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BioWorld - Saturday, June 20, 2026
Home » Topics » Europe, BioWorld

Europe, BioWorld
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Novel coronavirus SARS-CoV-2 spike protein

COVID-19 vaccines: European biopharma trio, Biontech-led programs racing ahead

April 23, 2020
By Nuala Moran
LONDON – A veteran of the European vaccines industry has brought together three companies in three countries, in what is described as an ultra-fast-track COVID-19 vaccine development program. From a standing start less than three months ago, the three biotechs, Reithera Srl in Rome, Leukocare AG in Munich, Germany, and Univercells SA in Brussels, Belgium, have advanced to GMP manufacturing, with first-in-human studies due to start in June.
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Capsule with Swiss flag

Swiss biotech investment slipped 25% in 2019 as sector braced for COVID-19 disruption

April 21, 2020
By Cormac Sheridan
DUBLIN – The Swiss biotech sector raised about CHF1.2 billion ($$1.2 billion) in equity investment in 2019, a significant downward dip on the last two years, but well ahead of its average annual raise of CHF800 million over the past decade, according to the newly published Swiss Biotech Report 2020.
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United Kingdom flag, map

U.K. pitches £500M bailout for VC-backed firms

April 20, 2020
By Nuala Moran
LONDON – The U.K. treasury announced a £500 million (US$622.5 million) COVID-19 bailout plan for research-based startups, which could see the government holding equity stakes in venture capital-backed firms.
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WHO headquarters, Geneva

EU leaders pan Trump’s move to halt U.S. funding as WHO updates COVID-19 response plan

April 15, 2020
By Nuala Moran
LONDON - The director general of the World Health Organization has given a dignified and measured response to President Donald Trump’s decision to halt U.S. funding of WHO, pending a review of its handling of the coronavirus pandemic.
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European Union map and coronavirus

EMA activates COVID-19 pandemic task force to galvanize European regulatory response

April 9, 2020
By Cormac Sheridan
DUBLIN – The EMA has activated a COVID-19 task force to coordinate and accelerate the European regulatory response to the pandemic. The task force is intended to take a lead role in shaping the development, authorization and post-approval surveillance of drugs and vaccines for treating or preventing COVID-19 infection.
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Two arrows in opposite directions

Ferrari, ERC part ways after only months, dispute over COVID-19 response

April 8, 2020
By Nuala Moran
LONDON – An unseemly row has broken out at the heart of EU science, with Mauro Ferrari, head of the European Research Council (ERC), accusing the European Commission of failing to coordinate and fund R&D needed to combat COVID-19.
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Cancer Research UK

U.K. research sees ‘substantial’ cuts to charity-funded research due to COVID-19

April 7, 2020
By Nuala Moran
LONDON – COVID-19 is posing a real threat to the viability of medical charities in the U.K., which collectively fund 17,000 scientists and invest more than £1.3 billion (US$1.6 billion) per annum in research.
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Virtual meetings illustration
Bio-Europe Spring 2020

Conferences go virtual, postpone, as COVID-19 spreads and Bio-Europe Spring wraps up

March 27, 2020
By Karen Carey
The five-day Bio-Europe Spring 2020 conference, possibly the first ever life sciences partnering event staged in an all-virtual format, ended on Friday, March 27, with high hopes that the industry would return to face-to-face interactions next year in Barcelona.
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Flag of China and masks
Bio-Europe Spring 2020

Closing panel offers COVID-19 lessons to learn from China

March 27, 2020
By Karen Carey
Biopharma industry leaders in China who were the first to experience the chaos of the COVID-19 pandemic shared their thoughts during a closing plenary session of the virtual Bio-Europe Spring 2020 meeting.
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Zolgensma product packaging

CHMP nods through multiple applications during virtual March meeting

March 27, 2020
By Cormac Sheridan
DUBLIN – Novartis AG, Bristol Myers Squibb Co. and Sanofi SA were among firms that secured positive opinions from EMA’s Committee for Medicinal Products for Human Use (CHMP) on marketing authorization applications for new therapies, which will progress to formal approvals 67 days from now. Because of the COVID-19 pandemic, the committee’s March meeting was held virtually.
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