Nanomedicines and Nanosimilars—Why a Robust Centralised Regulatory Framework Is Essential to Enhance Patient Safety

Michael P. Isles

Open source

DOI: 10.3389/fphar.2021.787239
Published: 2022-02-24
Container: Frontiers in Pharmacology
Publisher: Frontiers Media SA
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.3389/fphar.2021.787239,
  title = {Nanomedicines and Nanosimilars—Why a Robust Centralised Regulatory Framework Is Essential to Enhance Patient Safety},
  author = {Michael P. Isles},
  year = {2022},
  journal = {Frontiers in Pharmacology},
  doi = {10.3389/fphar.2021.787239},
  url = {https://doi.org/10.3389/fphar.2021.787239}
}

RIS

TY  - JOUR
TI  - Nanomedicines and Nanosimilars—Why a Robust Centralised Regulatory Framework Is Essential to Enhance Patient Safety
AU  - Michael P. Isles
PY  - 2022
JO  - Frontiers in Pharmacology
DO  - 10.3389/fphar.2021.787239
UR  - https://doi.org/10.3389/fphar.2021.787239
ER  -

APA

Isles, M. P. (2022). Nanomedicines and Nanosimilars—Why a Robust Centralised Regulatory Framework Is Essential to Enhance Patient Safety. Frontiers in Pharmacology. https://doi.org/10.3389/fphar.2021.787239

Source records

crossref · retrieved 2026-09-26T22:33:15.058Z