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Individual DNA passport could result in fewer drug side effects
You may be required to show a DNA passport when you pick up medicines at the pharmacy in the future. According to a new study, patients might suffer 30% fewer s...
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Marie Gårdmark: New incentives for orphan products on its way
"Let’s hope that the learnings from development of new therapies for rare diseases will spill over to more common conditions, orphan products paving the wave fo...
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Dryg fördubbling av restanmälda läkemedel
Antalet restanmälda läkemedel mer än fördubblades i fjol jämfört med föregående år, visar en sammanställning från Läkemedelsverket.
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3D-skanning av transparenta objekt
Användningen av 3D-skanning för transparenta och blanka objekt spelar en avgörande roll inom en snabbt växande industriell sektor. Inom områden som logistik, de...
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AZ får godkänt för läkemedel mot ovanlig sjukdom – kan minska beroendet av kortison
Astra Zenecas läkemedel Fasenra får utökad indikation i EU och blir nu godkänd som behandling mot den ovanliga autoimmuna sjukdomen känd som Churg-Strauss syndrom.
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Han får vetenskapspris för upptäckten av den inflammatoriska reflexen
Den amerikanske neurokirurgen och uppfinnaren Kevin J. Tracey tilldelas Hans Wigzells Forskningsstiftelses vetenskapliga pris på 100 000 dollar. Han får det bla...
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The government proposes fines for pharmaceutical companies that fail to notify drug shortages in time
According to a compilation from the Swedish Medicines Agency, the number of residually notified medicines increased by 54 % in Sweden last year compared to the ...
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The first pharmaceutical for eosinophilic esophagitis approved in the U.S.
The U.S. Drug Administration has approved the drug Dupixent (dupilumab) to treat inflammation of the oesophagus of the type eosinophil esophagitis.
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APL satsar på 3D-printing av extemporeläkemedel – klart med finländsk leverantör
Det blir det finländska healthtechbolaget Curify Labs Oy som tillverkar APL:s första 3D-printrar för tillverkning av extemporeläkemedel.
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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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Trends and overview: ELRIG "Robotics and Automation"
Laboratories on the way to end-to-end automation: Robotics, artificial intelligence and automation technology boosted by pandemic
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Decades of research destroyed at KI – a hacker attack cannot be ruled out!
Years of research, together with half a billion Swedish krona, went up in smoke when the freezers at Karolinska Institutet overheated. The breakdown has now bee...
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KI:s frysfiasko utrett: En kedja av brister
Det var en kedja av både tekniska och organisatoriska brister som tillsammans orsakade fryshaveriet på Karolinska institutet under julhelgen, då över 47 000 pro...
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Study names with an attitude – more important than you might think
Ironman, T-rex, Star-Trek. Popcorn, Proper, Scout. Nope, these are neither fantasy films nor dog names. They’re the names of ongoing cancer studies in Sweden.
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ALS – When the body has given up, but the brain persists
The nerve disease ALS gradually deprives the patient of control over the muscles and, eventually, also of speech. The eyes continue to function, though, and wit...
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Cytel Inc acquires the SDS Group
The multinational statistical software developer and contract research organization Cytel Inc, headquartered in Massachusetts, USA, acquires the Swedish consult...
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New drug alert in the US: Rise in overdoses linked to the use of drugs for animals
A combination of the synthetic drugs fentanyl and xylazine, an animal tranquilizer, has been labelled a “growing threat” by the White House due to its role in t...
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He is zooming in on topical preparations
According to Zelmic CEO David Sagna, topical products in drug development is a growing market, and to keep pace with the development, the company is awaiting ap...
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Verktyg för hjärtklaffsreparation får godkännande av FDA
Hjärtklaffsverktyget Triclip från Abbott har fått godkänt av amerikanska läkemedelsmyndigheten FDA. Tekniken är speciellt designad för behandling läckage i trikuspidalklaffen.
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Swedish breakthrough in Alzheimer’s: “We can finally present great data”
Treatments for Alzheimer’s disease are currently among the hottest topics in drug development. Two Swedish research companies with high ambitions and successes ...
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Dödsfall efter genterapi – FDA stoppar klinisk studie
En klinisk genterapistudie utförd av Rocket Pharmaceuticals har stoppats av FDA sedan en av patienterna avlidit.
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He is heading a new company for the development of Coegin’s cancer drug
The biotechnology company Coegin Pharma places the development of its drug candidate AVX420 in a newly formed company, Avexxin Oncology, based in Norway, and Jo...
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"Are we doing business the wrong way around in the Life Science Sector?"
For the past 50 years we have created solutions for problems that we thought would solve the problems. Pharmaceuticals have created big block buster drugs which...
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Björn Arvidsson: “We need robust and recognized ecosystems for continued competitiveness”
“We have idea carriers and excellent innovation opportunities, and now we must invest in creating ecosystems that provide them with even better growth opportuni...