Risk-adapted monitoring is not inferior to extensive on-site monitoring: Results of the ADAMON cluster-randomised study

BACKGROUND: According to Good Clinical Practice, clinical trials must protect rights and safety of patients and make sure that the trial results are valid and interpretable. Monitoring on-site has an important role in achieving these objectives; it controls trial conduct at trial sites and informs t...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Clin Trials
Egile Nagusiak: Brosteanu, Oana, Schwarz, Gabriele, Houben, Peggy, Paulus, Ursula, Strenge-Hesse, Anke, Zettelmeyer, Ulrike, Schneider, Anja, Hasenclever, Dirk
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: SAGE Publications 2017
Gaiak:
Data Management and Trial Conduct
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5718334/
https://ncbi.nlm.nih.gov/pubmed/28786330
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1740774517724165
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