Cargando…
Critical Analysis and Quality Assessment of Nanomedicines and Nanocarriers in Clinical Trials: Three Years of Activity at the Clinical Trials Office
Investigational medicinal products submitted over the course of 3 years and authorized at the Clinical Trials Office of the Italian Medicines Agency as part of a request for authorization of clinical trials were scrutinized to identify those encompassing nanomedicines. The quality assessment reports...
Autores principales: | Dri, Diego Alejandro, Gaucci, Elisa, Torrieri, Ilaria, Carafa, Maria, Marianecci, Carlotta, Gramaglia, Donatella |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318126/ https://www.ncbi.nlm.nih.gov/pubmed/35890333 http://dx.doi.org/10.3390/pharmaceutics14071438 |
Ejemplares similares
-
Surfactants, Nanomedicines and Nanocarriers: A Critical Evaluation on Clinical Trials
por: Dri, Diego Alejandro, et al.
Publicado: (2021) -
Quality Assessment of Investigational Medicinal Products in COVID-19 Clinical Trials: One Year of Activity at the Clinical Trials Office
por: Dri, Diego Alejandro, et al.
Publicado: (2021) -
Nanomedicines and nanocarriers in clinical trials: surfing through regulatory requirements and physico-chemical critical quality attributes
por: Dri, Diego Alejandro, et al.
Publicado: (2022) -
Regulatory Considerations on the use of Machine Learning based tools in Clinical Trials
por: Massella, Maurizio, et al.
Publicado: (2022) -
Smart Nanovesicles for Drug Targeting and Delivery
por: Marianecci, Carlotta, et al.
Publicado: (2019)