http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8140303-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_20b3abeba6114f2270183ba2cc9fc3fd
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-94
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-50
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filingDate 2008-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee10c05ae5a886d86619b55918b6515a
publicationDate 2012-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8140303-B2
titleOfInvention Bioequivalence evaluation method of evaluating bioequivalence of a generic drug to the corresponding original drug
abstract [Problem] There is provided a bioequivalence evaluation method not only of evaluating bioequivalence between an original drug and a corresponding generic drug but also of enabling to compare bioequivalence between generic drugs. n [Means of Solving the Problem] The bioequivalence between generic drugs is evaluated according to the Expression (1) wherein CCV Cmax g stands for the calibration coefficient of variation of Cmax (the maximum blood concentration), CCV Tmax g stands for the calibration coefficient of variation of Tmax (the time to maximum blood concentration), CCV T1/2 g stands for the calibration coefficient of variation of the half-life (T 1/2 ), and CCV AUC g stands for the calibration coefficient of variation of AUC (the blood concentration-area under the curve).
priorityDate 2008-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 27.