Determining topical product bioequivalence with stimulated Raman scattering microscopy
Author:
Funder
US FDA
Publisher
Elsevier BV
Reference66 articles.
1. A new paradigm for topical generic drug products: impact on therapeutic access;Raney;J. Am. Acad. Dermatol.,2020
2. Generic drugs in the United States: policies to address pricing and competition;Gupta;Clin. Pharmacol. Ther. (St. Louis, MO, U. S.),2019
3. Fda approval and regulation of pharmaceuticals, 1983-2018;Darrow;Jama,2020
4. The implications of regulatory framework for topical semisolid drug products: from critical quality and performance attributes towards establishing bioequivalence;Ilic;Pharmaceutics,2021
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1. Locally acting dermatology drug products: Pharmaco-analytic considerations for bioequivalence;European Journal of Pharmaceutical Sciences;2024-08
2. Innovative Approaches for Drug Discovery: Quantifying Drug Distribution and Response with Raman Imaging;Analytical Chemistry;2024-04-16
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