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dc.contributor.authorIrish Medicines Board (IMB)
dc.date.accessioned2011-02-03T17:34:23Z
dc.date.available2011-02-03T17:34:23Z
dc.date.issued2010-09-14
dc.identifier.urihttp://hdl.handle.net/10147/121059
dc.language.isoenen
dc.publisherIrish Medicines Board (IMB)en
dc.relation.ispartofseriesSUR-G0023-1en
dc.subjectMEDICAL EQUIPMENTen
dc.subjectDRUGen
dc.subjectREGULATIONen
dc.titleGuide to reporting of quality defects in medicinal products for human and veterinary useen
dc.typeGuidelineen
refterms.dateFOA2018-08-22T10:40:40Z


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