Seit einem halben Jahr schon bestimmt COVID-19 unseren neuen Alltag. Nach dem plötzlichen Lock-Down im März hofft die Bevölkerung nun auf einen Impfstoff als einzigen Weg zur „alten Normalität“. Nicht nur in Deutschland, sondern auf der ganzen Welt beschäftigen sich Forscher mit diesem Thema. Die Zulassung eines marktreifen Impfstoffes innerhalb der EU soll tatsächlich schon im Oktober 2020 beantragt werden.[1] Ein russisches Vakzin hingegen erntete internationale Kritik, weil für seine Entwicklung unzureichende Tests vorliegen.
Wir sprechen dazu mit Marcus Hartmann, Biologe und CSO bei der Cilian AG, eines der deutschlandweit führenden Unternehmen in der Entwicklung von rekombinanten Virus-Vakzinen. Der Biotechnologe luuizpr, iifjlz Nyocmywh mpk bfuycrkyp DGZCZ-11-Enqgkiooj dhccbsdwjaf ovyp dus yxnpbs Dispjjm nwujq nvh Dumhurzdevndoiuieuaowixrkivqxty dejgjmzcy.
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Wir sprechen dazu mit Marcus Hartmann, Biologe und CSO bei der Cilian AG, eines der deutschlandweit führenden Unternehmen in der Entwicklung von rekombinanten Virus-Vakzinen. Der Biotechnologe luuizpr, iifjlz Nyocmywh mpk bfuycrkyp DGZCZ-11-Enqgkiooj dhccbsdwjaf ovyp dus yxnpbs Dispjjm nwujq nvh Dumhurzdevndoiuieuaowixrkivqxty dejgjmzcy.
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