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Avaldati juhend kliiniliste uuringute taotluste kiiremaks hindamiseks

Euroopa ravimiametite koostöövõrgustiku (HMA) kliiniliste uuringute koordineerimisrühm (CTCG) avaldas FAST-EU pilootprojekti raames uue lühijuhendi, mis selgitab võimalusi kliiniliste uuringute taotluste kiiremaks hindamiseks Euroopa Liidus.

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Ootame oma meeskonnaga liituma labori spetsialisti!

Töö sisuks on ravimite laboratoorne analüüs ja kvaliteedi hindamine, sealhulgas füüsikalis-keemiliste meetodite kasutamine. Spetsialist vastutab ka kvaliteedi-
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