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Patient-reported outcomes in the regulatory approval of medical devices

dc.contributor.authorCruz Rivera, Samantha
dc.contributor.authorDickens, Andrew P
dc.contributor.authorAiyegbusi, Olalekan Lee
dc.contributor.authorFlint, Rebecca
dc.contributor.authorFleetcroft, Camilla
dc.contributor.authorMcPherson, Duncan
dc.contributor.authorCollis, Philip
dc.contributor.authorCalvert, Melanie J
dc.date.accessioned2024-09-06T14:14:02Z
dc.date.available2024-09-06T14:14:02Z
dc.date.issued2021-11-16
dc.identifier.citationCruz Rivera S, Dickens AP, Aiyegbusi OL, Flint R, Fleetcroft C, McPherson D, Collis P, Calvert MJ. Patient-reported outcomes in the regulatory approval of medical devices. Nat Med. 2021 Dec;27(12):2067-2068. doi: 10.1038/s41591-021-01546-9.en_US
dc.identifier.issn1078-8956
dc.identifier.eissn1546-170X
dc.identifier.doi10.1038/s41591-021-01546-9
dc.identifier.pmid34785789
dc.identifier.urihttp://hdl.handle.net/20.500.14200/5665
dc.description.abstractNo abstract availableen_US
dc.language.isoenen_US
dc.publisherNature Publishing Companyen_US
dc.relation.urlhttps://www.nature.com/nm/en_US
dc.subjectPatients. Primary care. Medical profession. Forensic medicineen_US
dc.titlePatient-reported outcomes in the regulatory approval of medical devicesen_US
dc.typeCorrespondenceen_US
dc.source.journaltitleNature Medicineen_US
dc.source.volume27
dc.source.issue12
dc.source.beginpage2067
dc.source.endpage2068
dc.source.countryUnited States
rioxxterms.versionNAen_US
dc.contributor.affiliationUniversity of Birmingham; Medicines and Healthcare products Regulatory Agency (MHRA); Health Data Research UK; University Hospitals Birmingham NHS Foundation Trusten_US
oa.grant.openaccessnaen_US


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