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dc.rights.licenseopenen_US
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorSALVO, Francesco
IDREF: 221043470
dc.contributor.authorMICALLEF, Joelle
dc.contributor.authorLAHOUEGUE, Amir
dc.contributor.authorCHOUCHANA, Laurent
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorLETINIER, Louis
dc.contributor.authorFAILLIE, Jean-Luc
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorPARIENTE, Antoine
IDREF: 13395711X
dc.date.accessioned2023-11-06T16:17:46Z
dc.date.available2023-11-06T16:17:46Z
dc.date.issued2023-07-01
dc.identifier.issn1744-764Xen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/184632
dc.description.abstractEnArtificial intelligence (AI) based tools offer new opportunities for pharmacovigilance (PV) activities. Nevertheless, their contribution to PV needs to be tailored to preserve and strengthen medical and pharmacological expertise in drug safety. This work aims to describe PV tasks in which the contribution of AI and intelligent automation (IA) tools is required, in the context of a continuous increase of spontaneous reporting cases and regulatory tasks. A narrative review with expert selection of pertinent references was performed through Medline. Two areas were covered, management of spontaneous reporting cases and signal detection. The use of AI and IA tools will assist a large spectrum of PV activities, both in public and private PV systems, in particular for tasks of low added value (e.g. initial quality check, verification of essential regulatory information, search for duplicates). Testing, validating, and integrating these tools in the PV routine are the actual challenges for modern PV systems, to guarantee high-quality standards in terms of case management and signal detection.
dc.language.isoENen_US
dc.subject.enArtificial intelligence
dc.subject.enDigital twins
dc.subject.enExplainability
dc.subject.enHuman intelligence
dc.subject.enMachine learning
dc.subject.enRegulation
dc.subject.enSystem interoperability
dc.title.enWill the future of pharmacovigilance be more automated?
dc.title.alternativeExpert Opin Drug Safen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1080/14740338.2023.2227091en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed37435796en_US
bordeaux.journalExpert Opinion on Drug Safetyen_US
bordeaux.page541-548en_US
bordeaux.volume22en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue7en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamAHEADen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04272597
hal.version1
hal.date.transferred2023-11-06T16:17:48Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Expert%20Opinion%20on%20Drug%20Safety&rft.date=2023-07-01&rft.volume=22&rft.issue=7&rft.spage=541-548&rft.epage=541-548&rft.eissn=1744-764X&rft.issn=1744-764X&rft.au=SALVO,%20Francesco&MICALLEF,%20Joelle&LAHOUEGUE,%20Amir&CHOUCHANA,%20Laurent&LETINIER,%20Louis&rft.genre=article


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