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The implications of regulatory framework for topical semisolid drug products: From critical quality and performance attributes towards establishing bioequivalence
| Naziv: | The implications of regulatory framework for topical semisolid drug products: From critical quality and performance attributes towards establishing bioequivalence | Autori: | Ilić, Tanja   ; Pantelić, Ivana ; Savić, Snežana |
Godina: | 2021 | Publikacija: | Pharmaceutics | ISSN: | 1999-4923 Pharmaceutics Pretraži identifikator |
Izdavač: | MDPI AG | Tip rezultata: | Naučni članak | Kolacija: | vol. 13 br. 5 str. 710-710 | DOI: | 10.3390/pharmaceutics13050710 | WoS-ID: | 000662436800001 | Scopus-ID: | 2-s2.0-85106874541 | PMID: | 34068036 | PMCID: | PMC8152494 | URI: | https://farfar.pharmacy.bg.ac.rs/handle/123456789/3906 https://enauka.gov.rs/handle/123456789/520155 |
Projekat: | Ministarstvo prosvete, nauke i tehnološkog razvoja Republike Srbije, Ugovor br. 200161 (Univerzitet u Beogradu, Farmaceutski fakultet) (RS-200161) | M-kategorija: | 21aM21a - Vodeći međunarodni časopis kategorije M21a |
