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Medical Devices Directive
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#	Item
1	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, Add to Reading List Source URL: www.bundesaerztekammer.de Language: English - Date: 2014-10-01 03:09:29 Medical research Medicine Research European Union directives Clinical research Research ethics Medical technology Medical device Ethics committee Clinical Trials Directive Medical Devices Directive Medical ethics
2	EC Gertificate Product Service Full Quality Assurance System Directive 93l42lEEC on Medical Devices (MDD), Annex ll excluding (4) Add to Reading List Source URL: www.ergoline.com Language: English - Date: 2015-03-10 06:48:27 Product certification Standards organizations Technischer berwachungsverein TV SD MDD Business Economy
3	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 Gazette Add to Reading List Source URL: www.jazmp.si Language: English - Date: 2013-07-12 06:13:47 Pharmaceuticals policy Health Medical research Clinical Trials Directive Directive 2001/83/EC Good laboratory practice Marketing authorization Good Clinical Practice Directive European Pharmacopoeia Biopharmaceutical Pharmacovigilance European Medicines Agency
4	IMDRF Presentation - Jurisdictional update - EU Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2016-03-29 21:04:17 Medicine Medical technology European Union directives Medical equipment Technology Medical device Medical Devices Directive ISO 14971 Single Use Medical Device Reprocessing
5	IMDRF Presentation - Jurisdictional update - EU Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2015-09-07 20:17:27 Medicine Medical technology European Union directives Medical equipment Medical device Medical Devices Directive ISO 14971 Italian Device Registration
6	Conference report Conference Substance-based medical devices: An important part of self-care Add to Reading List Source URL: www.aesgp.eu Language: English Medical technology European Union Medical equipment Medical device Notified Body Medical Devices Directive European Medicines Agency Single Use Medical Device Reprocessing CE marking
7	Official Journal of the European Union EN Add to Reading List Source URL: www.cellforcure.com Language: English - Date: 2013-05-23 03:56:30 Research Health European Medicines Agency Good Clinical Practice Directive Directive 2001/83/EC Clinical Trials Directive Medicinal product Medical Devices Directive Medical device Clinical research Pharmaceuticals policy Medicine
8	CL1993L0042EN0050010.0001.3bi_cp 1..1 Add to Reading List Source URL: www.communityequipment.org.uk Language: English - Date: 2013-08-14 04:29:20 Technology Clinical research Health Medical technology Medical Devices Directive European Union Medical device Directive 75/318/EEC Directive 2001/83/EC Pharmaceuticals policy European Union directives Medicine
9	Medical Information Systems – guidance for qualification and classification of standalone software with a medical purpose Add to Reading List Source URL: lakemedelsverket.se Language: English - Date: 2013-01-31 07:31:38 Medical technology Medical equipment Pharmaceutical industry Validity Quality management Medical device Medical Devices Directive CE mark Validation Medicine Technology Health
10	EXEMPTIONS OF ROHS DIRECTIVE UPDATED 10 April 2015, the European Commission announced two amendments to Annex IV of medical devices, and monitoring and control instruments of DirectiveEU (RoHSIt shall ent Add to Reading List Source URL: www.tuv.com Language: English - Date: 2015-06-22 15:15:53

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