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Standard requirements for GCP-compliant data management in multinational clinical trials.
Ohmann C, Kuchinke W, Canham S, Lauritsen J, Salas N, Schade-Brittinger C, Wittenberg M, McPherson G, McCourt J, Gueyffier F, Lorimer A, Torres F; ECRIN Working Group on Data Centres. Ohmann C, et al. Among authors: canham s. Trials. 2011 Mar 22;12:85. doi: 10.1186/1745-6215-12-85. Trials. 2011. PMID: 21426576 Free PMC article.
Sharing and reuse of individual participant data from clinical trials: principles and recommendations.
Ohmann C, Banzi R, Canham S, Battaglia S, Matei M, Ariyo C, Becnel L, Bierer B, Bowers S, Clivio L, Dias M, Druml C, Faure H, Fenner M, Galvez J, Ghersi D, Gluud C, Groves T, Houston P, Karam G, Kalra D, Knowles RL, Krleža-Jerić K, Kubiak C, Kuchinke W, Kush R, Lukkarinen A, Marques PS, Newbigging A, O'Callaghan J, Ravaud P, Schlünder I, Shanahan D, Sitter H, Spalding D, Tudur-Smith C, van Reusel P, van Veen EB, Visser GR, Wilson J, Demotes-Mainard J. Ohmann C, et al. Among authors: canham s. BMJ Open. 2017 Dec 14;7(12):e018647. doi: 10.1136/bmjopen-2017-018647. BMJ Open. 2017. PMID: 29247106 Free PMC article.
An iterative and interdisciplinary categorisation process towards FAIRer digital resources for sensitive life-sciences data.
David R, Ohmann C, Boiten JW, Abadía MC, Bietrix F, Canham S, Chiusano ML, Dastrù W, Laroquette A, Longo D, Mayrhofer MT, Panagiotopoulou M, Richard AS, Goryanin S, Verde PE. David R, et al. Among authors: canham s. Sci Rep. 2022 Dec 5;12(1):20989. doi: 10.1038/s41598-022-25278-z. Sci Rep. 2022. PMID: 36470968 Free PMC article.
84 results