Nanomedicines and Nanosimilars—Why a Robust Centralised Regulatory Framework Is Essential to Enhance Patient Safety
Author:
Publisher
Frontiers Media SA
Subject
Pharmacology (medical),Pharmacology
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3. Regulatory assessment of nano-enabled health products in public health interest. Position of the scientific advisory board of the French National Agency for the Safety of Medicines and Health Products;Frontiers in Public Health;2023-03-02
4. Nanomedicines and nanocarriers in clinical trials: surfing through regulatory requirements and physico-chemical critical quality attributes;Drug Delivery and Translational Research;2022-11-30
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