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Getinge and Neobiomics received Swecare's export awards
Two companies received awards during Swecare's annual conference.
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Region hävde avtalet – endoskopicentrum i konkurs
Uppgifter om att koloskopier utförts av ”okvalificerad personal” gjorde att Västra Götalandsregionen hävde avtalet med en privat vårdgivare. Nu har företaget i fråga inlett konkurs.
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Astra Zeneca faces potential multimillion-dollar fines in China
Astra Zeneca could be forced to pay up up to $8 million in fines for allegedly unpaid import duties in China, as the company seeks to rebuild trust following earlier controversies.
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Pulsen på patientförbunden del 5: Hjärt- och lungsjukdomar
Sjukvården behöver ha ett ökat fokus på individens enskilda behov och samordna sig mer mellan specialist- och primärvård. Det framhåller Riksförbundet Hjärt Lungs ordförande Anders Åkesson i Life Science Swedens artikelserie Pulsen på patientförbunden.
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Merck KGaA acquires American company in €3.0 billion deal
Germany’s Merck is completing the acquisition of Springwork Therapeutics for 3 billion euros.
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Attana-kund i USA drar ner – men projekten fortsätter
Forskningsbolaget Attana meddelar att projekt med bolagets teknologi kommer att fortsätta framåt, trots omfattande nedskärningar hos en av bolagets större forskningskunder i USA.
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Eli Lilly requests re-examination of Alzheimer's drug recommendation
Eli Lilly has requested that the EMA re-examine its opinion on the company's Alzheimer's drug, Kisunla, the agency announced on Friday.
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Mikael Kubista back with new venture after turbulent exit
Entrepreneur and researcher Mikael Kubista is starting a new company. Now he is also free to comment on the sequence of events that led to him losing ownership of his life's work – the company Tataa Biocenter. “Not only did they take our company away from us. They followed up by showering us with lawsuits,” he says.
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Bud på Biotage – värderas till över 11 miljarder
Uppsalabaserade Biotage meddelade på tisdagen att det amerikanska investmentbolaget KKR har lagt ett kontantbud på biotechbolaget.
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Kennedy: FDA är en ”marionett” åt läkemedelsindustrin
USA:s nya hälsominister Robert F. Kennedy Jr höll i fredags tal inför läkemedelsmyndigheten FDA:s medarbetare – och tog tillfället i akt att kalla dem för marionetter åt läkemedelsindustrin.
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New moves around Nykode's management – withdrawal of resignations
Norwegian Nykode Therapeutics is reinstating members of the management team who previously announced their resignations.
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After the threat of tariffs – Novartis invests 230 billion in the USA
Pharmaceutical giant Novartis plans to invest 23 billion dollarsover the next five years to expand its production in the USA. The goal is for all medicines destined for the US market to be produced within the country.
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FDA plans to replace animal testing with AI – “Paradigm shift”
The requirement for animal testing in drug development will be phased out and replaced by AI, according to an announcement by the FDA. The decision has been met with skepticism from the National Association for Biomedical Research.
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”AI-teknologin är här – dags för industrin att ta rygg på Läkemedelsverket”
När Läkemedelsverket, som en av de första läkemedelsmyndigheterna i Europa, lanserade sin egen generativa AI-lösning – den lokalt driftade Regulus – sattes ett nytt riktmärke för hela branschen. Detta visar tydligt att det går att förena innovation och teknikutveckling med strikt regulatorisk efterlevnad, skriver Andreas Palmlund, expert på AI i reglerade miljöer på Coeye, i en debattartikel.
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From pharmacist to life science podcaster – Magnus Lejelöv uses his voice as a tool
Magnus Lejelöv has more than 20 years of experience in the pharmaceutical industry and has conducted nearly two hundred interviews with healthcare professionals on his podcasts.
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Korbinian Löbmann leads scientific meeting on drug formulation: High activity in the field
Korbinian Löbmann has moderated New Updates in Drug Formulation & Bioavailability several times before. Now he is once again taking on the scientific meeting. Life Science Sweden reached out to him.
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EQT säljer Karo Healthcare för 27 miljarder
Riskkapitalbolaget KKR förvärvar det svenska konsumenthälsobolaget Karo Healthcare från EQT.
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Tau-targeted Alzheimer's drug gets Fast Track designation in the USA
Biogen's Alzheimer's candidate BIIB080 has been granted Fast Track designation by the U.S. Food and Drug Administration (FDA).
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New drug to simplify treatment of hemophilia
A new type of treatment for hemophilia, which only needs to be administered every two months, has been approved by the U.S. Food and Drug Administration (FDA).
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FDA’s Top Vaccine Official resigns – Issues sharp criticism of Kennedy
FDA’s Top Vaccine Official is leaving his post while simultaneously criticizing the country’s health secretary for allowing “misinformation and lies” to influence his views on vaccine safety.
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Nytt läkemedel ska förenkla behandling av blödarsjuka
En ny typ av behandling mot hemofili, som bara behöver ges varannan månad, har godkänts av den amerikanska läkemedelsmyndigheten FDA.
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Success for Genmab's antibody-drug conjugate
The Danish company Genmab has received Japanese approval for its treatment for advanced or recurrent cervical cancer.
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Vaccine skeptic David Geier to lead study on link to autism
The American government is to launch a study on whether vaccines cause autism – and has appointed a well-known vaccine skeptic to lead the analysis.
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Several departures at the top at Nykode
Members of both the management and the board are leaving the Norwegian biotech company Nykode.
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