Cargando…
The general data protection regulation, the clinical trial regulation and some complex interplay in paediatric clinical trials
Although a number of authors have commented upon the impact of the GDPR on clinical trial conduct, few have examined the specific setting of paediatric trials. Whilst the general principles are the same as those for adults, some additional considerations arise. The ages of consent relating to data p...
Autor principal: | Dalrymple, H. W. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8032631/ https://www.ncbi.nlm.nih.gov/pubmed/33462697 http://dx.doi.org/10.1007/s00431-021-03933-3 |
Ejemplares similares
-
Informed consent and assent guide for paediatric clinical trials in Europe
por: Lepola, Pirkko, et al.
Publicado: (2022) -
Patient Protection in Clinical Trials in India: Some Concerns
por: Srinivasan, Sandhya
Publicado: (2010) -
Some data quality issues at ClinicalTrials.gov
por: Chaturvedi, Neha, et al.
Publicado: (2019) -
Standardising Outcomes in Paediatric Clinical Trials
por: Clarke, Mike
Publicado: (2008) -
Analysis of Paediatric Clinical Trial Characteristics and Activity Over 23 Years—Impact of the European Paediatric Regulation on a Single French Clinical Research Center
por: Arnadottir, Johanna, et al.
Publicado: (2022)