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A Model Data Management Plan Standard Operating Procedure: Results From the DIA Clinical Data Management Community, Committee on Clinical Data Management Plan.
Brand, Scott; Bartlett, Diana; Farley, Mary; Fogelson, Miriam; Hak, Jan Bart; Hu, Grace; Montana, Olivia D; Pierre, Jan Holladay; Proeve, Johann; Qureshi, Samina; Shen, Anita; Stockman, Peter; Chamberlain, Richard; Neff, Kristin.
Afiliação
  • Brand S; 1 QPS LLC, Newark, DE, USA.
  • Bartlett D; Committee chair.
  • Farley M; 2 Theravance Biopharma US Inc, South San Francisco, CA, USA.
  • Fogelson M; 3 KAI Research Inc, Rockville, MD, USA.
  • Hak JB; 3 KAI Research Inc, Rockville, MD, USA.
  • Hu G; 4 QPS LLC, Groningen, The Netherlands.
  • Montana OD; 5 QPS Qualitix, Taipei, Taiwan, ROC.
  • Pierre JH; 6 SyneractHCR Inc, San Diego, CA, USA.
  • Proeve J; 7 INC Research, Orlando, FL, USA.
  • Qureshi S; 8 Bayer Healthcare, Leverkusen, Germany.
  • Shen A; 9 PSI International Inc, Rockville, MD, USA.
  • Stockman P; 10 Janssen of Johnson & Johnson, Beijing, China.
  • Chamberlain R; 11 Merck, Sharp and Dohme, Oss, The Netherlands.
  • Neff K; 12 Extended Clinical Services LLC, Centreville, VA, USA.
Ther Innov Regul Sci ; 49(5): 720-729, 2015 Sep.
Article em En | MEDLINE | ID: mdl-30227041
ABSTRACT

BACKGROUND:

The DIA Clinical Data Management Community created a committee to develop a model standard operating procedure (SOP) for writing a data management plan.

METHODS:

The goal of the committee was to develop a plan that could be used by industry and academic institutions. The model was based on contributed examples from committee members and their experiences with current practices and technologies. It is understood that as new clinical trial technology is implemented, the SOP will require modification.

RESULTS:

The model SOP and associated templates are presented as a starting point, and each company or institution will need to modify them to meet its individual needs.

CONCLUSION:

The model DMP SOP produced addresses most data management issues that are present in any phase clinical trial while providing a flexible framework.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article