Publicación:
“Review: Application of Bioequivalence Testing of Medicines in Peru“

dc.contributor.authorAlvarado, Angel T.
dc.contributor.authorGray, Vivian
dc.contributor.authorMuñoz, Ana María
dc.contributor.authorSaravia, María
dc.contributor.authorBendezú, María R.
dc.contributor.authorChávez, Haydee
dc.contributor.authorGarcía, Jorge A.
dc.contributor.authorYbañez-Julca, Roberto
dc.contributor.authorChonn-Chang, Andres
dc.contributor.authorBasurto, Patricia
dc.contributor.authorPineda-Pérez, Mario
dc.contributor.authorSalazar, Alberto
dc.date.accessioned2023-03-08T15:56:23Z
dc.date.available2023-03-08T15:56:23Z
dc.date.issued2022-11
dc.description.abstract“This is a review of the current status of drug bioequivalence studies in Peru. A bibliographic search was conducted in PubMed (Medline database) for bioequivalence studies in Peru. Generic drugs constitute the basis of pharmacological requests in health care systems in Latin American countries. Peru has enacted laws and regulations that require bioequivalence studies of high health risk drugs and exemptions, based on international legislation, to be conducted in research centers accredited by the authority of Health. There is a list of 19 drugs that must demonstrate their therapeutic equivalence through in vivo or in vitro studies, of which 13 have shown bioequivalence in vivo, and 8 of those have shown bioequivalence in vitro. There is a challenge for health authorities to enforce the current legislation and an even greater challenge for pharmaceutical laboratories to demonstrate bioequivalence of multi-source drugs with the reference drug. “es_ES
dc.formatapplication/pdf
dc.identifier.doidx.doi.org/10.14227/DT290422P220es_ES
dc.identifier.urihttps://hdl.handle.net/20.500.13053/7979
dc.language.isoenges_ES
dc.publisherDissolution Technologies Inces_ES
dc.publisher.countryUSes_ES
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectBioequivalence, multi-source drug, reference drug, drug regulation, in vitro testinges_ES
dc.subject.ocdehttp://purl.org/pe-repo/ocde/ford#3.03.00
dc.title“Review: Application of Bioequivalence Testing of Medicines in Peru“es_ES
dc.typeinfo:eu-repo/semantics/article
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dspace.entity.typePublication

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