API/FDF Analytical Testing Site

Known as: API/FDF Analytical Testing, Active Pharmaceutical Ingredient / Finished Dosage Form Analytical Testing Site, Analytical Testing 
Sites that perform testing of the characteristics and attributes of active pharmaceutical ingredients or finished dosage forms.
National Institutes of Health

Papers overview

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2015
2015
Many international organisations encourage studies in a sex-gender perspective. However, research with a gender perspective… (More)
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2009
2009
Pharmaceutical regulatory agencies are increasingly concerned with trace-level genotoxic impurities in drug substances, requiring… (More)
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Review
2008
Review
2008
BACKGROUND Cardiac troponin is the biomarker of choice for the serologic diagnosis of acute coronary syndromes. International… (More)
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2008
2008
Residual host cell protein impurities (HCPs) are a key component of biopharmaceutical process related impurities. These… (More)
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2007
2007
The behavior of ion-exchange chromatography is well understood with respect to changes in ionic strength, pH, resin ligand… (More)
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2006
2006
The ability of the API Coryne system, version 2.0, to identify 178 strains of gram-positive rods was evaluated. Seventy eight… (More)
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2003
2003
Chemical imaging technology is a rapid examination technique that combines molecular spectroscopy and digital imaging, providing… (More)
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Highly Cited
2001
Highly Cited
2001
A method has been established and validated for identification and quantification of individual, as well as total, anthocyanins… (More)
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2001
2001
The API 50CH and API ZYM systems fulfil an important role in the polyphasic taxonomic identification of lactobacilli. When the… (More)
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1998
1998
Dynamic measurements of exocytosis have been difficult to perform in intact epithelial monolayers. We have designed a system that… (More)
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