Toxicity of excipients--a Food and Drug Administration perspective.
about
Comparative Risk Assessment of Formulation Changes in Generic Drug Products: A Pharmacology/Toxicology PerspectiveImportance and globalization status of good manufacturing practice (GMP) requirements for pharmaceutical excipientsIdentification of phthalates in medications and dietary supplement formulations in the United States and CanadaNonclinical vehicle use in studies by multiple routes in multiple species.Tolerable Levels of Nonclinical Vehicles and Formulations Used in Studies by Multiple Routes in Multiple Species With Notes on Methods to Improve Utility.GC-MS analysis of ethanol and other volatile compounds in micro-volume blood samples--quantifying neonatal exposure.Developmental toxicity assessment of common excipients using a stem cell-based in vitro morphogenesis model.Trends in excipient safety evaluation.
P2860
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P2860
Toxicity of excipients--a Food and Drug Administration perspective.
description
2003 nî lūn-bûn
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2003年の論文
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年學術文章
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2003年學術文章
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name
Toxicity of excipients--a Food and Drug Administration perspective.
@en
Toxicity of excipients--a Food and Drug Administration perspective.
@nl
type
label
Toxicity of excipients--a Food and Drug Administration perspective.
@en
Toxicity of excipients--a Food and Drug Administration perspective.
@nl
prefLabel
Toxicity of excipients--a Food and Drug Administration perspective.
@en
Toxicity of excipients--a Food and Drug Administration perspective.
@nl
P2860
P1476
Toxicity of excipients--a Food and Drug Administration perspective.
@en
P2093
Norman A See
Robert E Osterberg
P2860
P304
P356
10.1177/109158180302200507
P577
2003-09-01T00:00:00Z