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dc.contributor.authorHealth Service Executive
dc.date.accessioned2021-10-13T16:10:47Z
dc.date.available2021-10-13T16:10:47Z
dc.date.issued2021-10
dc.identifier.urihttp://hdl.handle.net/10147/630608
dc.description• Introduction Mark Turner, Chair of the HSE Medical Device Regulations Steering Group • HPRA Perspective Andrew Dullea , Regulatory & Policy Assessor | Medical Devices, Health Products Regulatory Authority • HSE Perspective Ger Flynn, National Clinical Lead for Medical Devices • Key Messages for Hospitals Ciaran Browne, Acute Operations • Q & A Stephen McGrath, Communications • Close Mark Turner, Chair of the HSE Medical Device Regulations Steering Groupen_US
dc.language.isoenen_US
dc.publisherHealth Service Executiveen_US
dc.subjectPatient Safetyen_US
dc.subjectQUALITYen_US
dc.subjectMEDICAL DEVICESen_US
dc.titleMedical Device Regulations Updateen_US
dc.typePresentationen_US
refterms.dateFOA2021-10-13T16:10:47Z


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