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dc.contributor.authorIrish Medicines Board (IMB)
dc.date.accessioned2010-04-14T14:46:56Z
dc.date.available2010-04-14T14:46:56Z
dc.date.issued2002-11-06
dc.identifier.urihttp://hdl.handle.net/10147/96526
dc.language.isoenen
dc.publisherIrish Medicines Board (IMB)en
dc.subjectMEDICAL EQUIPMENTen
dc.subjectREGULATIONen
dc.titleGuidance notes for manufacturers on clinical investigations carried out in Irelanden
dc.typeOtheren
refterms.dateFOA2018-09-03T10:52:05Z


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