A missing link in the bench-to-bedside paradigm: engaging regulatory stakeholders in clinical genomics research

For genomic medicine research to be fully translated into clinical care, it is critical for researchers to engage stakeholders who ultimately regulate the use of genomic technologies and therapeutics within healthcare practice. Herein, we describe an example of how this might work.

Detalles Bibliográficos
Autores principales: O’Daniel, Julianne M., Berg, Jonathan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031300/
https://www.ncbi.nlm.nih.gov/pubmed/27655359
http://dx.doi.org/10.1186/s13073-016-0351-7
Descripción
Sumario:For genomic medicine research to be fully translated into clinical care, it is critical for researchers to engage stakeholders who ultimately regulate the use of genomic technologies and therapeutics within healthcare practice. Herein, we describe an example of how this might work.