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BioWorld - Sunday, April 12, 2026
Home » Topics » Europe, BioWorld

Europe, BioWorld
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US, Switzerland on path to share GMP inspection findings

Jan. 17, 2023
After years of negotiations, the U.S. FDA and Swissmedic are one step away from recognizing each other’s good manufacturing practice (GMP) inspections of biopharma facilities.
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New EU stockpile to prepare for CBRN events

Jan. 17, 2023
The European Commission is spending €242 million (US$261 million) to create the first rescEU strategic reserve of chemical, biological, radiological and nuclear (CBRN) medical countermeasures.
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Vaccine and data illustration

Biontech teams up with UK for personalized mRNA cancer vaccines

Jan. 6, 2023
By Nuala Moran
Biontech SE is piggybacking on the U.K.’s lead in implementing cancer genomics in routine health care to set up a national clinical trial of personalized mRNA cancer vaccines that are based on the mutational landscape of individual tumors.
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Clinical trial virtual display

EMA moving ahead with clinical trial system despite industry concern

Jan. 6, 2023
By Nuala Moran
The EMA will require all new clinical trial applications to be submitted via its clinical trials information system after Jan. 31, 2023, despite pharma companies and other users raising concerns about functionality and technical failures they are experiencing with the system.
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Downward-arrow-on-EU-flag-and-chart.png

The year of the squeeze: Europe equity funding drops 55% to $6.8B in 2022

Jan. 6, 2023
By Cormac Sheridan
For European biotechnology, 2022 was a year of contraction. Disclosed equity investments in European firms engaged in the discovery and development of therapeutics totaled $6.782 billion, down 55% on the previous year’s record-breaking tally of $15.193 billion. Last year’s tally is the worst performance since 2017 and is well below the totals achieved during the two years immediately preceding the onset of the COVID-19 pandemic, which triggered a boom in biotech investing.
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Ukrainian and Russian flags painted on cracked concrete

Russia imposing its regulatory framework on Ukrainian territories

Dec. 28, 2022
By Mari Serebrov
Although the war is still raging in Ukraine, Russia is marching forward with asserting its regulatory framework on health care in the parts of Ukraine it’s claiming as the spoils of the war it started 11 months ago.
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Map of Ukraine and Russia

Top Trends of 2022: European pharma embroiled in turmoil of Ukraine war in 2022

Dec. 28, 2022
By Richard Staines
It was a year of turmoil in Europe as Russia’s invasion of Ukraine and the fall-out from the COVID-19 pandemic shaped the fortunes of the life sciences industry in 2022. After years of tension, Russia’s attempt to annex Ukraine on Feb. 24 caused outrage and disruption and was unanimously opposed on humanitarian grounds by the life sciences and pharma industry.
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ABPI looks to new settlement to tame UK drug rebates

Dec. 28, 2022
By Mari Serebrov
Facing a 26.5% rebate on 2023 sales of branded prescription drugs in the U.K., the Association of the British Pharmaceutical Industry (ABPI) is seeking talks with the government early in the new year to develop a new biopharma settlement for the future that will reflect the potential of the life sciences sector to drive improvements in the health and economy of the U.K.
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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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