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                             21 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Access to clinical trial data—Commentary Devereaux, PJ
2019
16 5 p. 552-554
artikel
2 A novel, hybrid, single- and multi-site clinical trial design for CLN3 disease, an ultra-rare lysosomal storage disorder Adams, Heather R
2019
16 5 p. 555-560
artikel
3 Creation of an institutional semi-independent data monitoring committee Tannock, Lisa R
2019
16 5 p. 523-530
artikel
4 Design and analysis of a clinical trial using previous trials as historical control Schoenfeld, David Alan
2019
16 5 p. 531-538
artikel
5 Detection of atypical data in multicenter clinical trials using unsupervised statistical monitoring Trotta, Laura
2019
16 5 p. 512-522
artikel
6 Editorial Begg, Colin B
2019
16 5 p. 446
artikel
7 Ethical complexities of responding to bystander risk in HIV prevention trials Eyal, Nir
2019
16 5 p. 458-460
artikel
8 Facebook advertising for recruitment of midlife women with bothersome vaginal symptoms: A pilot study Guthrie, Katherine A
2019
16 5 p. 476-480
artikel
9 Impact of retrospective data verification to prepare the ICON6 trial for use in a marketing authorization application Embleton-Thirsk, Andrew
2019
16 5 p. 502-511
artikel
10 Objective monitoring of mosquito bednet usage and the ethical challenge of privacy revelations about study bystanders: Ethical analysis Fairchild, Amy L
2019
16 5 p. 469-472
artikel
11 Objective monitoring of mosquito bednet usage and the ethical challenge of respecting study bystanders’ privacy Krezanoski, Paul
2019
16 5 p. 466-468
artikel
12 Open science: The open clinical trials data journey Rockhold, Frank
2019
16 5 p. 539-546
artikel
13 Organ donor intervention trials and risk to bystanders: An ethical analysis Cohen, Ivan Glenn
2019
16 5 p. 463-465
artikel
14 Organ donor intervention trials and the ethical challenge of bystander organ recipients Kimmelman, Jonathan
2019
16 5 p. 461-462
artikel
15 Recruitment and retention: A randomized controlled trial of video-enhanced versus standard consent processes within the E-OPTIMAL study Brubaker, Linda
2019
16 5 p. 481-489
artikel
16 Regulating impact on bystanders in clinical trials: An unsettled frontier Eyal, Nir
2019
16 5 p. 450-454
artikel
17 Research methodology and practical issues relating to the conduct of a medical device registry Bisdas, Theodosios
2019
16 5 p. 490-501
artikel
18 Risk to bystanders in clinical trials: A symposium Eyal, Nir
2019
16 5 p. 447-449
artikel
19 Sex partners as bystanders in HIV prevention trials: Two test cases for research ethics Bärnighausen, Till
2019
16 5 p. 455-457
artikel
20 The ethical relevance of two types of adverse health effects on research bystanders as applied to HIV, mosquito bednet and organ transplant trials Vong, Gerard
2019
16 5 p. 473-475
artikel
21 Transparency and objectivity in governance of clinical trials data sharing: Current practices and approaches Shabani, Mahsa
2019
16 5 p. 547-551
artikel
                             21 gevonden resultaten
 
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