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Astra Zenecas Fasenra floppade i KOL-studie
Astra Zenecas astmaläkemedel Fasenra misslyckades i en studie som utvärderade behandlingen för patienter med kronisk obstruktiv lungsjukdom, KOL.
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Astra Zenecas Fasenra floppade i KOL-studie
Astra Zenecas astmaläkemedel Fasenra misslyckades i en studie som utvärderade behandlingen för patienter med kronisk obstruktiv lungsjukdom, KOL.
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Astra Zeneca nådde fas III-mål med ny blodtrycksbehandling
Astra Zeneca rapporterar nya positiva data för baxdrostat mot svårbehandlat högt blodtryck.
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Automated nitrogen analysis reduces costs per sample
N-Realizer analytical system from C. Gerhardt increases productivity with valve block from Festo
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Automated nitrogen analysis reduces costs per sample
N-Realizer analytical system from C. Gerhardt increases productivity with valve block from Festo
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Optimism hos Astra Zeneca efter positiv astmastudie
Nya, positiva studieresultat gör att Astra Zeneca hoppas på ett utvidgat användningsområde för astmaläkemedlet Airsupra.
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Scale Up Your Image Analysis
ZEISS arivis Hub for accelerated analysis and faster results.
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Sustainability at Festo
On the Way to the Net Zero Era - New Sustainability Report published
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Licensavtal tar Astra Zeneca in i kampen om fetmapatienterna
Astra Zeneca ger sig nu på allvar in på det allt hetare fetmaområdet genom ett licensavtal med kinesiska Eccogene.
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Large study on milk: Risky for women but not for men
The risk of ischemic heart disease (IHD) and acute myocardial infarction (MI) increased for women with milk intake levels higher than 2 glasses per day, while n...
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Webinar: How to Plan And Analyze a Real-World Evidence Study
This webinar is for drug developers who want to understand the basic ideas of analyzing an RWE study, as well as avoiding the most common pitfalls.
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Webinar: Clinical evaluation and clinical investigation of medical devices
Whether you are a small medtech company or a large one, this webinar is a must-attend for anyone curious about how clinical studies on medical devices are conducted.
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Webinar: Medtech quality and regulatory compliance
This webinar is for you who are developing or planning to develop a medical device, combination, or borderline product. In one hour, we will discuss what you ne...
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Webinar: What is Regulatory Affairs?
This webinar is intended for those who work within the life science sector and would like to gain a general understanding of regulatory affairs for human medicinal products.
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Clean solutions - Handling viscose substances with precision
Laboratories in the chemical, petrochemical, pharmaceutical and food technology industries are increasingly relying on automation for sample preparation. The Mo...
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Medicover expanderar i Norge – köper fertilitetsklinker
Vård- och diagnostikföretaget Medicover, baserat i Stockholm, har köpt 70 procent av röstandelarna i den norska fertilitetsverksamheten Klinikk Hausken. Det är ...
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Anna Törner: The clinical trial – Periscope to reality
What happens to the patients in the clinical trial is not very interesting, writes Anna Törner in a column.
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Postdoc på spel i Astra Zenecas internationella tävling
Eslövsbon Cátia Bonito Ferreira ska på onsdag presentera sitt forskningsförslag om behandling för en sällsynt sjukdom inför en jury i hopp om att få en betald p...
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Founder of Bioarctic, Lars Lannfelt, is honoured: “I want to create something for the future”
It´s like a scientist’s dream: to be the world’s first with a drug that genuinely affects one of our major diseases. Lars Lannfelt and his company Bioarctic hav...
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De håller koll efter transplantation
Genom att följa virusinfektion kan sjukhusen förebygga komplikationer.
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Upcoming event: New updates on drugs
At Medicon Valley Alliance venues in Copenhagen/Örestad April 1 2020 the meeting New updates in Drug Formulation & Bioavailability takes place for the for the eighth time.
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Investments worth 40 billion in the Öresund region – “A huge investment wave”
A new report reveals that medical companies in the Oresund region are investing like never before.
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Biosimilars bring price pressure, but are they sufficiently used?
When biosimilars were introduced just over 16 years ago, hopes were raised that they would give many more patients access to effective but otherwise extremely e...
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Marie Gårdmark: Big data evidence generation drives change in the EU regulatory system
Rapid developments in technology have led to the possibility for the generation and analysis of vast volumes of data. Will the availability of big data lead to ...