Hai cercato la traduzione di have you participated in clinical... da Danese a Italiano

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

statistical principles for clinical trials
statistical principles for clinical trials

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

statistical principles for veterinary clinical trials
statistical principles for veterinary clinical

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

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.

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

bearbejdet efter "prevention of coronary heart disease in clinical practice:
17 warfarina la contemporanea somministrazione di {nome di fantasia} e warfarina ha dato luogo ad una piccola diminuzione del tempo di protrombina durante i primi giorni di terapia che si è normalizzato entro 15 giorni di trattamento con {nome di fantasia}.

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.

points to consider concerning endpoints in clinical studies with haematopoietic growth factors for mobilisation of autologous stem cells
factors for mobilisation of autologous stem cells points to consider on the clinical investigation of new medicinal products for

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

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.

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).

appendix to the nfg on the clinical investigation of medicinal products in the treatment of schizophrenia (cpmp/ ewp/ 559/ 95) – methodology of clinical trials concerning the development of depot preparations of approved medicinal products in schizophrenia.
appendix to the nfg on the clinical investigation of medicinal products in the treatment of schizophrenia (cpmp/ ewp/ 559/ 95) – methodology of clinical trials concerning the development of depot preparations of approved medicinal products in schizophrenia.

appendix to the note for guidance on the clinical investigation of medicinal products in the treatment of schizophrenia (cpmp/ ewp/ 559/ 95) – methodology of clinical trials concerning the development of depot preparations of approved medicinal products in schizophrenia.
appendix to the note for guidance on the clinical investigation of medicinal products in the treatment of schizophrenia (cpmp/ ewp/ 559/ 95) – methodology of clinical trials concerning the development of depot preparations of approved medicinal products in schizophrenia.

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.