Results 211 to 220 of about 7,041 (257)

Time series analysis of the new tiering pricing policy for generic medicines in South Korea. [PDF]

Front Pharmacol
Park CM, Song I, Kim DS.
europepmc   +1 more source

US Antibiotic Importation and Supply Chain Vulnerabilities.

JAMA Health Forum
Socal MP, Sun Y, Ballreich JM, Lambert JD, Dai T, Dada M.   +5 more
europepmc   +1 more source

Cost-Efficient and Fast At-Line Assessment of Content and Uniformity in Low-Dose Dimdazenil Capsules Using Transmission Raman Spectroscopy. [PDF]

Pharmaceutics
Ma X, Shan L, Zhu S, Zhu Z, Lu S, Xu M, Yin L.   +6 more
europepmc   +1 more source

Pharmaceutical Co-Crystal Formulation of Rivaroxaban with Niacinamide: Preparation, Characterization, and In Vitro Release Evaluation. [PDF]

Materials (Basel)
Solomon C, Sarbu I, Anuța V, Ozon EA, Musuc AM, Rusu A, Surdu VA, Chandak A, Gavriloaia RM, Fița AC, Nită DT, Mitu MA.   +11 more
europepmc   +1 more source

Methods of Thermal Analysis as Fast and Reliable Tools for Identification and Quantification of Active Ingredients in Commercially Available Drug Products. [PDF]

Pharmaceutics
Wesolowski M.
europepmc   +1 more source

Contemporary Techniques and Prospects in Pharmaceutical Tablet Surface Analysis. [PDF]

ACS Meas Sci Au
Finšgar M.
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Study on the Adsorption Behavior of Preservatives in Multidose Eye Drops and Their Interaction with Packaging Materials. [PDF]

ACS Omega
Guan H, Han X, Sun J, Wang J, Ning B, Sun H, Zhao X.   +6 more
europepmc   +1 more source

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Stable isotopic composition of the active pharmaceutical ingredient (API) naproxen

Journal of Pharmaceutical and Biomedical Analysis, 2005
A survey of the multi-stable isotopic composition of an active pharmaceutical ingredient (API), naproxen, was performed to assess the potential of Isotope Ratio Mass Spectrometry (IRMS) to distinguish the provenance of APIs. Twenty-six lots of naproxen from six manufacturers representing four countries (Italy, India, Ireland, and the USA) were analyzed
A M, Wokovich, J A, Spencer, B J, Westenberger, L F, Buhse, J P, Jasper   +4 more
exaly   +3 more sources

A quality evaluation strategy for multi-sourced active pharmaceutical ingredient (API) starting materials

Journal of Pharmaceutical and Biomedical Analysis, 2006
Establishing appropriate impurity specifications for active pharmaceutical ingredient (API) starting materials is an important component of the commercialization and registration of an API. Multiple sources and routes of manufacture of starting materials and the capability of the API synthetic process for tolerating impurities introduced with starting ...
Peter F, Gavin, Bernard A, Olsen, David D, Wirth, Kurt T, Lorenz   +3 more
exaly   +3 more sources