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![]() Date: 2012-03-12 12:41:45Evaluation Reference Standards Law Medical Devices Directive CE mark Regulation (EU) No 305/2011 Toy safety Clinical Trials Directive Pharmaceuticals policy European Union directives Clinical research | Add to Reading List |
![]() | Response of the German Medical Association to the proposal by the European Commission for a Regulation of the European Parliament and of the Council on medical devices, and amending DirectiveEC,DocID: 1rdN0 - View Document |
![]() | EC Gertificate Product Service Full Quality Assurance System Directive 93l42lEEC on Medical Devices (MDD), Annex ll excluding (4)DocID: 1r3Af - View Document |
![]() | The Agency for Medicinal Products and Medical Devices of the Republic of Slovenia has prepared the unofficial consolidated text for the Medicinal Products Act which includes: Medicinal Products Act (Official GazetteDocID: 1r1yj - View Document |
![]() | IMDRF Presentation - Jurisdictional update - EUDocID: 1r0Yg - View Document |
![]() | IMDRF Presentation - Jurisdictional update - EUDocID: 1quqf - View Document |