Vous avez cherché: randomised clinical trials (Danois - Italien)

statistical principles for clinical trials
statistical principles for clinical trials

statistical principles for veterinary clinical trials
statistical principles for veterinary clinical

choice of control group in clinical trials
choice of control group in clinical trials

points to consider on multiplicity issues in clinical trials.
points to consider on multiplicity issues in clinical trials.

points to consider on missing data points to consider on multiplicity issues in clinical trials
points to consider on missing data

position paper on the non- clinical safety studies to support clinical trials with a single low dose of a compound
position paper on the non-clinical safety studies to support clinical trials with a single low dose of a compound

patienternes responsrate blev vurderet ved brug af aids clinical trials group (actg) - kriterier for læsionsrespons ved ks.
i valori relativi alla velocità di risposta dei pazienti sono stati valutati usando i criteri dell’ aids clinical trials group (actg) per le risposte delle lesioni nel sk.

concept paper on the development of a cpmp points to consider on methodological issues in confirmatory clinical trials with flexible design and analysis plan.
concept paper on the development of a cpmp points to consider on methodological issues in confirmatory clinical trials with flexible design and analysis plan.

denne udtalelse var for mig afgørende for min indstilling til clinical trial directive.
questa affermazione ha rappresentato per me uno spunto importante quando ho dovuto decidere la mia posizione sulla clinical trial directive.

lad os glemme alt om at oprette denne european clinical trials platform og i stedet støtte det panafrikanske netværk amvtn, som netop står over for at blive omdannet til en fond.
lasciamo stare la creazione di questa european clinical trials platform e appoggiamo invece la rete panafricana amvtn, che sta per essere trasformata in un fondo.

generelt skal de kliniske undersøgelser udføres som kontrollerede kliniske forsøg (controlled clinical trials) og sä vidt muligt randomiserede; enhver anden metode skal begrundes.
in generale, le prove cliniche devono essere effettuate sotto forma di "controlled clinical trials" (prove cliniche controllate) e, ove possibile, randomizzate; va giustificata ogni altra forma di prova.

concept paper on the development of an appendix to the cpmp note for guidance on the clinical investigation of medicinal products in the treatment of schizophrenia, on methodology of clinical trials concerning the development of depot preparations of approved medicinal products in schizophrenia
concept paper on the development of an appendix to the cpmp note for guidance on the clinical investigation of medicinal products in the treatment of schizophrenia, on methodology of clinical trials concerning the development of depot preparations of approved medicinal products in schizophrenia

ud fra denne logik bør man også især genoverveje, om og på hvilke betingelser forskere og læger bør have adgang til de informationer om kliniske forsøg, der findes i european clinical trials database (eudract database).
in tale logica andrà ripensato in particolare se e con quali modalità si debbano rendere disponibili anche agli sperimentatori e ai medici le informazioni relative agli studi clinici presenti nell'european clinical trials database (eudract).

titel på dokumentet position paper on the non- clinical safety studies to support clinical trials with a single low dose of a compound note for guidance on specification limits for residues of metal catalysts note for guidance on comparability of medicinal products containing biotechnology- derived proteins as drug substance:
titolo del documento position paper on the non-clinical safety studies to support clinical trials with a single low dose of a compound note for guidance on specification limits for residues of metal catalysts note for guidance on comparability of medicinal products containing biotechnology-derived proteins as drug substance:

den samlede analyse af paediatric aids clinical trials group (pactg) ’ s protokoller 245, 356, 366, 377 og 403 tillod evaluering at pædiatriske patienter yngre end 3 måneder (n=17) i disse pactg - studier.
l’ analisi consolidata dei protocolli di gruppi di studi clinici in pazienti pediatrici con aids (pactg) 245, 356, 366, 377 e 403 ha consentito la valutazione di pazienti pediatrici con meno di 3 mesi di età (n=17) arruolati in questi studi pactg.