Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Johann Proeve"'
Autor:
Philipp Bruland, Mark McGilchrist, Eric Zapletal, Dionisio Acosta, Johann Proeve, Scott Askin, Thomas Ganslandt, Justin Doods, Martin Dugas
Publikováno v:
BMC Medical Research Methodology, Vol 16, Iss 1, Pp 1-10 (2016)
Abstract Background Data capture is one of the most expensive phases during the conduct of a clinical trial and the increasing use of electronic health records (EHR) offers significant savings to clinical research. To facilitate these secondary uses
Externí odkaz:
https://doaj.org/article/bfbfc36e140849ccb5427a836149ea84
Autor:
Kaye H Fendt, Samina Qureshi, Johann Proeve, Ariana Winder, Dale Plummer, Nimita Limaye, Mary Banach
Publikováno v:
Journal of the Society for Clinical Data Management. 1
In the United States, clinical data management (CDM) has been accelerating from a single focus on collecting and preparing clinical trial data for study analysis to a multi-pronged endeavor. This endeavor emphasizes quality data from inception or pla
Autor:
Mary Farley, Miriam Fogelson, Jan Bart Hak, Kristin Neff, Scott Brand, Jan Holladay Pierre, Peter Stockman, Grace Hu, Johann Proeve, Olivia D. Montana, Samina Qureshi, Anita Shen, Diana Bartlett, Richard Chamberlain
Publikováno v:
Therapeutic innovationregulatory science. 49(5)
The DIA Clinical Data Management Community created a committee to develop a model standard operating procedure (SOP) for writing a data management plan. The goal of the committee was to develop a plan that could be used by industry and academic insti
Autor:
Alphonse Mordiva, Mats Sundgren, Robert Ferendo, Hans Eriksson, Emma Witch, Peter Bachmann, Kathe Balinski, Taru Blom, Kerstin Forsberg, Leslie Thomas, Diane King, Martin Simán, Norbert Bleich, Johann Proeve, Laszlo Vasko
Publikováno v:
Therapeutic innovationregulatory science. 49(1)
Although much information is already available publically from information-sharing initiatives such as ClinicalTrials.gov, information about clinical programs is unstructured, inconsistent, and incomplete. Clinical research within bioscience companie
Autor:
Martin Dugas, Justin Doods, Eric Zapletal, Philipp Bruland, Johann Proeve, Thomas Ganslandt, Mark McGilchrist, Scott Askin, Dionisio Acosta
Publikováno v:
BMC Medical Research Methodology, Vol 16, Iss 1, Pp 1-10 (2016)
BMC Medical Research Methodology
BMC Medical Research Methodology
Background Data capture is one of the most expensive phases during the conduct of a clinical trial and the increasing use of electronic health records (EHR) offers significant savings to clinical research. To facilitate these secondary uses of routin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::985637cc28afb7401b0f26b920c84c94
https://opus4.kobv.de/opus4-fau/frontdoor/index/index/docId/8023
https://opus4.kobv.de/opus4-fau/frontdoor/index/index/docId/8023
Autor:
Danielle Dupont, Mats Sundgren, Johann Proeve, Andreas Schmidt, Ariel Beresniak, Mats Ericson, Dipak Kalra, Elena Bolanos, Georges De Moor, Nadir Ammour
Publikováno v:
Journal of Health & Medical Informatics. 7
Background: The new technological platform developed by the Electronic Health Records for Clinical Research (EHR4CR) European research project (2011-2016) has been specially designed to enable the trustworthy reuse of health data contained in hospita
Autor:
Ariel Beresniak, Danielle Dupont, Mats Sundgren, Mats Ericson, Georges De Moor, Neelam Patel, Johann Proeve, Elena Bolanos, Nadir Ammour, Toeresin Karakoyun, Pascal Coorevits, Dipak Kalra, Andreas Schmidt
Publikováno v:
Contemporary clinical trials. 46
Introduction The widespread adoption of electronic health records (EHR) provides a new opportunity to improve the efficiency of clinical research. The European EHR4CR ( Electronic Health Records for Clinical Research ) 4-year project has developed an
Autor:
Johann Proeve
Clinical data management is faced with an ever growing number of data from clinical trials which need to be looked at by critically reviewing the necessity of the data captured, by standardizing the clinical trial set up as much as possible, and by u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76604738272e5e0a96d31545adafe1f6
https://doi.org/10.1016/b978-0-12-420246-7.00022-0
https://doi.org/10.1016/b978-0-12-420246-7.00022-0
Autor:
Danielle Dupont, Neelam Patel, Ariel Beresniak, Johann Proeve, Nadir Ammour, Mats Sundgren, Mats Ericson, G. De Moor, Andreas Schmidt, Elena Bolanos, Dipak Kalra
Publikováno v:
Value in Health. 17:A630