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European Pharmaceutical Review

@PharmaReview

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The leading FREE journal for up-to-the-minute information and news on all aspects of drug analysis, formulation, delivery, manufacturing and regulation.

United Kingdom
Joined April 2010
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@PharmaReview
European Pharmaceutical Review
6 months
According to analysis by @moderna_tx, 20 percent of participants in UK industry-sponsored clinical research were enrolled in a Moderna trial in 2023/2024.
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The announcement follows the completed construction of Moderna’s MITC and progress in its long-term partnership with the UK government.
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@PharmaReview
European Pharmaceutical Review
6 months
“Excitingly, advances in gene editing are happening very rapidly. it seems likely that cheaper, safer and more effective forms of gene editing will emerge for sickle cell disease over the coming years,” commented Professor Rees of King’s College London.
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The committee’s approval of the one-time gene therapy means the healthcare inequalities in sickle cell disease can begin to be re-addressed.
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@PharmaReview
European Pharmaceutical Review
7 months
"This year’s figures demonstrate that biotech is a vibrant growth sector of the UK economy with an exceptional ability to attract global investment," says @BIA_UK's CEO.
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Cutting-edge science and large international investment are driving growth in the UK’s biotech sector, the organisation’s new report reveals.
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@PharmaReview
European Pharmaceutical Review
7 months
"With nearly two-thirds of all major #pharma company revenues set to come from dealmaking in the next five years, deals will remain at the centre of #lifesciences strategy," says @EYnews Global Life Sciences Deals Leader.
europeanpharmaceuticalreview.com
For a strong 2025, dealmaking should be central to the life sciences strategy, says EY’s annual M&A report.
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@PharmaReview
European Pharmaceutical Review
7 months
Oncology continues to be the dominant area in early-phase ATMP clinical trials for investigational therapies, the report data shows. #pharma #clinicaltrials
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Cell and Gene Therapy Catapult's (CGT Catapult) findings attest to the UK remaining “a highly attractive destination for clinical trials”.
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@PharmaReview
European Pharmaceutical Review
7 months
The new recommendations will support health technology assessment (HTA) and aid technology developers to provide data for evidence submissions.
europeanpharmaceuticalreview.com
The paper aims to support HTA decision making, considering “little change in guidance on the use of surrogate endpoints in HTA since 2018”.
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@PharmaReview
European Pharmaceutical Review
7 months
The acquisition will include rights to a TKI molecule, which according to @GSK's CSO, has potential to help close a major gap in the current standard of care of gastrointestinal stromal tumours.
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The new acquisition by GSK could enable major advancement in the standard of care for GIST after nearly two decades.
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@PharmaReview
European Pharmaceutical Review
7 months
Gene editing technologies are expected to innovate #pharma personalised medicine in 2025, says @ClarivateHealth 's latest Drugs to Watch report. #drugdevelopment.
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Eleven medicines are poised to make waves in the pharmaceutical industry in 2025, according to the report.
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@PharmaReview
European Pharmaceutical Review
8 months
As part of the agreement, @bmsnews is responsible for development and commercialisation of the novel antibodies and related products. #biologics #EPRtalks
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The agreement between BMS and BioArctic is set to advance development of anti-Aβ antibody therapies, which have shown benefit in Alzheimer's.
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@PharmaReview
European Pharmaceutical Review
8 months
"Approval by the [European Commission] is significant because Elahere is the first new medication approved specifically for platinum-resistant ovarian cancer since 2014". #pharma #EPRTalks
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Here, AbbVie's International Medical Affairs Head for Oncology discusses the significance of the EU approval of Elahere for ovarian cancer.
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@PharmaReview
European Pharmaceutical Review
8 months
"These reforms protect the safe development of pioneering new treatments," Dr June Raine, @MHRAgovuk Chief Executive stated. #EPRTalks.
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The amended regulatory framework will foster clinical trial design innovation and provide UK life sciences with faster trial approvals.
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@PharmaReview
European Pharmaceutical Review
8 months
“By combining our expertise in #clinicaltrials and #lifesciences with world-class researchers, we can accelerate the development of groundbreaking treatments that will benefit patients across [the UK and Switzerland]” says UK Health Minister. #EPRTalks
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The joint UK-Swiss agreement between two key players in life sciences, marks a long-term commitment to strengthening research in the sector.
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@PharmaReview
European Pharmaceutical Review
8 months
AD | Making spirits bright!. Save 25% and enjoy free gummi bears with our most popular nucleic purification kits. Whether you’re looking for #DNA, #RNA, or #plasmidpurification, clean-up for #NGS, gels, or PCR, we’ve got the perfect kit.
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@PharmaReview
European Pharmaceutical Review
9 months
The new appointments by @Amgen and @pfizer will drive development of new medicines across numerous therapeutic areas such as rare disease and cancer. #EPRTalks.
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The new executive appointments at Amgen and Pfizer will support advancement in therapeutic areas including oncology and rare disease.
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@PharmaReview
European Pharmaceutical Review
9 months
Investment in @sanofi's Lyon Gerland site will aid internal bioproduction of a type 1 #diabetes drug, enabling market availability in 2027. #pharmaceuticalmanfacturing #EPRTalks.
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This a bioproduction investment in Lyon, France supports Sanofi in its goals to lead in the immunology sector.
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@PharmaReview
European Pharmaceutical Review
9 months
As part of the acquisition, @BioNTech_Group will gain rights to a state-of-the-art biologics manufacturing facility. #biologics #EPRTalks.
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The acquisition is set to strengthen BioNTech’s capabilities in development and manufacture of next-generation bispecific antibodies.
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@PharmaReview
European Pharmaceutical Review
9 months
🚨 Last Chance! 🚨. Join us this week for a webinar with Vivien Knospe from FUJIFILM WAKO Chemicals on the Monocyte Activation Test (MAT)!. 📅 Register now: #mat #monocyteactivationtest #webinar
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@PharmaReview
European Pharmaceutical Review
9 months
A key benefit of the film bag “is its simplicity because no equipment for mechanical aeration is required”. #microbiology #EPRTalks
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The alternative liquid culturing method does not require shaking of microorganisms, according to the research.
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@PharmaReview
European Pharmaceutical Review
10 months
The drug candidate included in the @abbvie deal transports the antibody across the blood-brain barrier to enable degradation of amyloid beta plaque. #Alzheimers
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The deal will help AbbVie to strengthen its neuroscience pipeline, including aiding development of therapies for delivery into the CNS.
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@PharmaReview
European Pharmaceutical Review
10 months
Join Vivien Knospe from FUJIFILM WAKO Chemicals to discuss the Monocyte Activation Test (MAT)!. Learn about:.✅ MAT implementation in the EU.✅ Status in pharmacopoeias (USP, EP, JP, ChP).✅ Performing a MAT assay. 📅 Register now:
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