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Manual of Decisions for Implementation of Directive 98/8/EC concerning the placing on the market of biocidal products
Document date: Tue Dec 20 00:00:00 CET 2011 - Created by GROW.R.4 - Publication date: Mon May 18 15:36:01 CEST 2015
Information on the Customs Union Agreement with Turkey in the field of medical devices
Document date: Thu Feb 10 00:00:00 CET 2011 - Created by GROW.R.4 - Publication date: Wed May 13 08:50:35 CEST 2015 - Last update: Wed May 13 08:50:34 CEST 2015
Guidance document - Clinical investigation, clinical evaluation - Clinical investigations: serious adverse event reporting - MEDDEV 2.7/3
Document date: Tue Dec 28 00:00:00 CET 2010 - Created by GROW.DDG1.D.4 - Publication date: Tue Apr 26 14:48:57 CEST 2016
Guidance document Medical Devices - Clinical investigation, clinical evaluation - Guidelines on Clinical investigations: a guide for manufacturers and notified bodies - MEDDEV 2.7/4
Document date: Sun Dec 19 00:00:00 CET 2010 - Created by GROW.R.4 - Publication date: Mon May 18 13:02:02 CEST 2015 - Last update: Mon May 18 13:02:01 CEST 2015
Informative document of the Commission’s services on placing on the market of medical devices
Document date: Mon Nov 15 00:00:00 CET 2010 - Created by GROW.R.4 - Publication date: Wed May 13 08:14:33 CEST 2015
Guidance document - Classification of Medical Devices - MEDDEV 2.4/1 rev.9
Document date: Sat Jun 19 00:00:00 CEST 2010 - Created by GROW.R.4 - Publication date: Mon May 18 13:44:53 CEST 2015
Guidance document - Clinical investigation, clinical evaluation - Clinical evaluation: Guide for manufacturers and notified bodies - MEDDEV 2.7/1 rev.3
Document date: Sat Dec 19 00:00:00 CET 2009 - Created by GROW.R.4 - Publication date: Mon May 18 08:08:23 CEST 2015 - Last update: Mon May 18 08:08:22 CEST 2015
Guidance document - Scope, field of application, definition - Borderline products, drug-delivery products and medical devices incorporating, as integral part, an ancillary medicinal substance or an ancillary human blood derivative - MEDDEV 2.1/3 rev.3
Document date: Sat Dec 19 00:00:00 CET 2009 - Created by GROW.R.4 - Publication date: Mon May 18 10:00:12 CEST 2015
Information on the relation between the revised Directives 90/385/EEC and 93/42/EEC concerning (active implantable) medical devices and Directive 2006/42/EC on machinery
Document date: Thu Aug 20 00:00:00 CEST 2009 - Created by GROW.R.4 - Publication date: Wed May 13 07:16:31 CEST 2015
Information on the relation between the revised Directive 93/42/EEC concerning medical devices and Directive 89/686/EEC on personal protective equipment
Document date: Thu Aug 20 00:00:00 CEST 2009 - Created by GROW.R.4 - Publication date: Wed May 13 07:40:13 CEST 2015
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