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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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2016
2016
Proficiency testing (PT), also called external quality assessment, is an essential tool for quality assurance of the analytical… 
2009
2009
Three anhydrous polymorphs, a monohydrate and a dihydrate of an active pharmaceutical ingredient, N-{[(5S)-3-(4-{6-[(1R,5S)-6… 
2007
2007
The behavior of ion‐exchange chromatography is well understood with respect to changes in ionic strength, pH, resin ligand… 
Review
2000
Review
2000
BACKGROUND: Since 1989, the CDC's Model Performance Evaluation Program has shipped samples to voluntary participant laboratories… 
1988
1988
The enzymatic activities of 53 strains of Pseudomonas cepacia were determined by using the API ZYM system. Strong alkaline… 
1986
1986
Asbestos fiber counting data reported in the NIOSH Proficiency Analytical Testing (PAT) Program are used in this study to… 
Review
1960
Review
1960
In micronutrient deficiency experiments with plants the salts used to supply macronutrients must obviously be free of significant…