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Guidance Notes for Manufacturers of Class I Medical Devices
Electromagnetic Compatibility - Report on the Second Joint Cross-Border EMC Market Surveillance Campaign on domestic power tools (2007/08)
R&TTE directive - Guide to the R&TTE Directive 1999/5/EC
Fertilisers - Communication from the Commission - Guide to the compilation of a technical file on application to designate a fertiliser as ‘EC fertiliser’
Guidance document - Committees/Working Groups contributing to the implementation of the Medical Device Directives - MEDDEV 2.15 rev.3
Guidance document Medical Devices - Clinical investigation, clinical evaluation - Guide for Competent Authorities in making an assessment of clinical investigation notification - MEDDEV 2.7/2
Chemicals - Drug precursors - Guidance document agreed between the Commission services and the competent authorities of Member States on the implementation of the Community legislation on drug precursors -Version 2
Directive 2006/42/EC - Management of the Machinery Directive
Guidance note: labelling of ingredients in cosmetics directive 76/768/EEC - update February 2008
R&TTE directive - Obligations associated with the placing on the market of radio equipment and telecommunications terminal equipment
Directive 2000/14/EC - Quick guide to using Noise
Guidance document on administrative cooperation in the area of market surveillance of cosmetic products - Version of 01.06.2007
Guidance document - In vitro diagnostic medical devices - Supply of Instructions For Use (IFU) and other information for In-vitro Diagnostic (IVD) Medical Devices - MEDDEV 2.14/3 rev.1
Guidance document on Directive 2005/50/EC on the reclassification of hip, knee and shoulder joint replacements
Guidance note: the “restricted fields of application” for coloring agents in annex IV to cosmetics directive 76/768/EEC
Guiding principles for the content of Particular material appraisal - Pressure equipment (PE 03-28)
Directive 76/769/EEC - Guidance Document on the interpretation of the concept “which can be placed in the mouth” as laid down in the Annex to the 22nd amendment of Council Directive 76/769/EEC
Guidance note: the restriction to “professional use” in the cosmetics directive 76/768/EEC - version 1.0 (December 2005)
Guidance document on the demarcation between the cosmetic products Directive 76/768 and the medicinal products Directive 2001/83 as agreed between the commission services and the competent authorities of Member States
Pressure Equipment Directive - Guiding Principles for the contents of European Approval of Materials (EAM) drafts (version approved at the WGP on 17 March 2004)
Guidance document - In vitro diagnostic medical devices - Research Use Only products - MEDDEV 2.14/2 rev.1
Guidance document - Conformity assessment procedure - Evaluation of medical devices incorporating products containing natural rubber latex - MEDDEV 2.5/9 rev.1
Position paper on guidelines for the application of the European Parliament and Council Directive 2000/14/EC
Guidance document - Notified bodies - Designation and monitoring of Notified Bodies within the framework of EC Directives on Medical devices - MEDDEV 2.10/2 rev.1
Good Environmental Practice in the European Extractive Industry: a Reference Guide
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