Cargando…
Mapping of the available standards against the regulatory needs for nanomedicines
Appropriate documentary standards and reference materials are crucial building blocks for the development of innovative products. In order to support the emerging sector of nanomedicine, relevant standards must be identified and/or developed before the products will enter into the regulatory approva...
Autores principales: | Halamoda‐Kenzaoui, Blanka, Holzwarth, Uwe, Roebben, Gert, Bogni, Alessia, Bremer‐Hoffmann, Susanne |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585614/ https://www.ncbi.nlm.nih.gov/pubmed/29923692 http://dx.doi.org/10.1002/wnan.1531 |
Ejemplares similares
-
Main trends of immune effects triggered by nanomedicines in preclinical studies
por: Halamoda-Kenzaoui, Blanka, et al.
Publicado: (2018) -
Bridging communities in the field of nanomedicine
por: Halamoda-Kenzaoui, Blanka, et al.
Publicado: (2019) -
Toxic effects of nanomaterials for health applications: How automation can support a systematic review of the literature?
por: Halamoda‐Kenzaoui, Blanka, et al.
Publicado: (2021) -
The agglomeration state of nanoparticles can influence the mechanism of their cellular internalisation
por: Halamoda-Kenzaoui, Blanka, et al.
Publicado: (2017) -
Future perspectives for advancing regulatory science of nanotechnology-enabled health products
por: Halamoda-Kenzaoui, Blanka, et al.
Publicado: (2022)