Cargando…
Input analysis for two public consultations on the EU Clinical Trials Regulation
BACKGROUND: The European Union’s (EU) Clinical Trials Directive was replaced by an EU-Regulation as of 2016. The policy revision process was subject to a formal impact assessment exercised by the European Commission (EC) from 2008 to 2014. Following the EU principles of Good Governance, deliberation...
Autores principales: | Langhof, Holger, Lander, Jonas, Strech, Daniel |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027082/ https://www.ncbi.nlm.nih.gov/pubmed/27639695 http://dx.doi.org/10.1186/s12961-016-0141-0 |
Ejemplares similares
-
Implementation of data access and use procedures in clinical data warehouses. A systematic review of literature and publicly available policies
por: Pavlenko, Elena, et al.
Publicado: (2020) -
Empirical studies on how ethical recommendations are translated into practice: a cross-section study on scope and study objectives
por: Schwietering, Johannes, et al.
Publicado: (2023) -
Involving patients and the public in medical and health care research studies: An exploratory survey on participant recruiting and representativeness from the perspective of study authors
por: Lander, Jonas, et al.
Publicado: (2019) -
Analysis of submissions to the EU’s public consultation on tobacco traceability and security features
por: Gallagher, Allen William Andrew, et al.
Publicado: (2021) -
Current Practice of Public Involvement Activities in Biomedical Research and Innovation: A Systematic Qualitative Review
por: Lander, Jonas, et al.
Publicado: (2014)