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1
Generic Drug Product Development: International Regulatory Requirements for Bioequivalence
Informa Healthcare
Isadore Kanfer (ed.)
,
Leon Shargel (ed.)
product
products
studies
bioequivalence
ihbk055
sph
reference
generic
drugs
dose
dosage
kanfer
pharmaceutical
count
clinical
char
dissolution
bioavailability
guidance
january
required
forms
formulation
active
subjects
medicines
oral
safety
administration
therapeutic
guidelines
cmax
innovator
countries
testing
regulatory
auc
accessed
efficacy
guideline
appropriate
formulations
analysis
criteria
vitro
pharmacokinetic
subject
parameters
equivalent
fda
Year:
2010
Language:
english
File:
PDF, 3.43 MB
Your tags:
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0
english, 2010
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