Cargando…
Risk-proportionate clinical trial monitoring: an example approach from a non-commercial trials unit
BACKGROUND: Some level of monitoring is usually required during a clinical trial to protect the rights and safety of trial participants and to safeguard the quality and reliability of trial results. Although there is increasing support for the use of risk-proportionate approaches to achieve these ai...
Autores principales: | Tudur Smith, Catrin, Williamson, Paula, Jones, Ashley, Smyth, Alan, Hewer, Simon Langton, Gamble, Carrol |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022377/ https://www.ncbi.nlm.nih.gov/pubmed/24739398 http://dx.doi.org/10.1186/1745-6215-15-127 |
Ejemplares similares
-
Reporting of harms outcomes: a comparison of journal publications with unpublished clinical study reports of orlistat trials
por: Hodkinson, Alex, et al.
Publicado: (2016) -
Indirect Comparisons: A Review of Reporting and Methodological Quality
por: Donegan, Sarah, et al.
Publicado: (2010) -
Interventions to improve recruitment and retention in clinical trials: a survey and workshop to assess current practice and future priorities
por: Bower, Peter, et al.
Publicado: (2014) -
The Role of Systematic Reviews in Pharmacovigilance Planning and Clinical Trials Authorisation Application: Example from the SLEEPS Trial
por: Gamble, Carrol, et al.
Publicado: (2013) -
Developing guidance for a risk-proportionate approach to blinding statisticians within clinical trials: a mixed methods study
por: Iflaifel, Mais, et al.
Publicado: (2023)