Биовейвер (Обзор регуляторных требований)

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in vitro



!

:
FDA ():
Waiver of In Vivo Bioavailability and Bioequivalence Studies for ImmediateRelease Solid Oral Dosage Forms Based on a Biopharmaceutics Classification
System 08/2000
EMEA ():
Note for guidance on the investigation of bioavailability and
bioequivalence /EWP/QWP/1401/98 26/07/2001
GUIDELINE ON THE INVESTIGATION OF BIOEQUIVALENCE (DRAFT)
CPMP/EWP/QWP/1401/98 Rev. 1 24.07.2008
FIP:

WHO:
WHO Technical Report Series 937
WHO EXPERT COMMITTEE ON SPECIFICATIONS FOR PHARMACEUTICAL
PREPARATIONS, Fortieth Report, 2006
+ 2 ():
190

17.04.2007

:
FDA:
http://www.fda.gov/cder/guidance/3618fnl.pdf
EMEA:
http://www.emea.europa.eu/pdfs/human/ewp/140198en.pdf
http://www.emea.europa.eu/pdfs/human/qwp/140198enrev1.pdf
FIP:
http://www.fip.org/www/index.php?page=ps_sig_bcs
WHO:
http://whqlibdoc.who.int/trs/WHO_TRS_937_eng.pdf
:
http://www.pharma-center.kiev.ua/view/new_doc


1.


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The R Project for Statistical Computing


S-Plus
SPSS
SAS
WinNonLin
Kinetica
EquivTest



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