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Incorporation of text recognition into trial it systems to safeguard against enrolment of ineligible patients or inappropriate reporting of adverse events

机译：将文本识别功能集成到试用版系统中，以防止不合格患者入组或不良事件的不当举报

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Martin Dennis; Rustam Salman; Gillian Mead; Connor McGill; David Perry;
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年度 2013
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1. Incorporation of text recognition into trial it systems to safeguard against enrolment of ineligible patients or inappropriate reporting of adverse events [J] . Martin Dennis, Rustam Salman, Gillian Mead, Trials . 2013,第SUPPLEMENTa1期

机译：将文本识别功能集成到试用系统中，以防止不合格患者入组或不良事件的不当举报
2. Reporting adverse events in cancer surgery randomized trials: A systematic review of published trials in oesophago-gastric and gynecological cancer patients [J] . Meghelli Leila, Narducci Fabrice, Mariette Christophe, Critical reviews in oncology/hematology . 2016,第Null期

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3. Reporting adverse events in cancer surgery randomized trials: A systematic review of published trials in oesophago-gastric and gynecological cancer patients [J] . Meghelli Leila, Narducci Fabrice, Mariette Christophe, Critical reviews in oncology/hematology . 2016,第Null期

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4. Toward User-Centered Patient Safety Event Reporting System: A Trial of Text Prediction in Clinical Data Entry [C] . Lei Hua, Yang Gong MEDINFO . 2015

机译：向用户居中的患者安全事件报告系统：临床数据进入中文本预测的试验
5. Hypersensitivity Adverse Event Reporting in Clinical Cancer Trials: Barriers and Potential Solutions to Studying Severe Events on a Population Level [D] . ?Eldredge, Christina 2020

机译：临床癌症试验中的超敏反不良事件报告：障碍和潜在的解决方案，用于研究人口水平的严重事件
6. Incorporation of text recognition into trial it systems to safeguard against enrolment of ineligible patients or inappropriate reporting of adverse events [O] . Martin Dennis, Rustam Salman, Gillian Mead, 2013

机译：将文本识别功能集成到试用版系统中以防止不合格患者入组或不良事件的不当举报
7. A tolerability burden index in schizophrenia: incorporating patient perspective in clinical trial adverse event reporting [O] . François, Clément, Guiraud-Diawara, Alice, Lançon, Christophe, 2017

机译：精神分裂症的耐受性负担指数：将患者观点纳入临床试验不良事件报告

Incorporation of text recognition into trial it systems to safeguard against enrolment of ineligible patients or inappropriate reporting of adverse events

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