New cancer drugs hit US market first
![Foto: Colourbox](https://photos.watchmedier.dk/watchmedier/resize:fill:3840:0:0/plain/https://photos.watchmedier.dk/Images/article6502361.ece/ALTERNATES/schema-16_9/USA%2520EU.jpg)
Six months. That is, on average, how much longer it takes for the European Medicines Agency, EMA, to approve new drugs to combat cancer compared with its US counterpart, FDA, according to a new survey.
Læs hele artiklen
Få adgang i 14 dage for 0 kr. Det kræver intet kreditkort, og du vil ikke overgå til et betalt abonnement efterfølgende.
Med din prøveperiode får du:
Få fuld adgang til dig og dine kollegaer
Start et gratis virksomhedsprøveabonnementRelaterede artikler
EMA wants clear guidelines for genomic biomarkers
For abonnenter
Pilot project: early access in the EU
For abonnenter