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dc.contributor.authorHealth Protection Surveillance Centre
dc.date.accessioned2022-01-24T10:59:58Z
dc.date.available2021-01-26T15:27:09Z
dc.date.available2021-04-13T10:58:46Z
dc.date.available2021-04-19T14:14:08Z
dc.date.available2021-04-23T09:51:58Z
dc.date.available2021-06-11T13:27:55Z
dc.date.available2021-07-07T13:42:53Z
dc.date.available2021-10-01T09:10:08Z
dc.date.available2021-10-13T09:12:41Z
dc.date.available2022-01-24T10:59:58Z
dc.date.issued2022-01-21
dc.identifier.urihttp://hdl.handle.net/10147/628851
dc.descriptionThese FAQs are based on HIQA evidence syntheses, public health and clinical evidence summaries which have informed the HIQA-Expert Advisory Group (EAG) available at https://www.hiqa.ie/areas-we-work/health-technology-assessment/covid-19-publications. They also include advice and decisions of the former COVID-19 EAG (Jan-Sept 2020) and the HSE Antigen Detection Testing (ADT) group.en_US
dc.language.isoenen_US
dc.publisherHealth Service Executiveen_US
dc.subjectCoronavirusen_US
dc.subjectCOVID-19en_US
dc.subjectINFECTION PREVENTION AND CONTROLen_US
dc.subjectPUBLIC HEALTHen_US
dc.titleCOVID-19: Frequently Asked Questions: asymptomatic infection, re-infection, immunity, and GP management of patients with COVID-19 test results from a laboratory other than the public laboratory service. [v2.4]en_US
dc.typeOtheren_US
refterms.dateFOA2021-01-26T15:27:10Z


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