Europass also matches user skills and interests such as location and topic to success suitable jobs. The CE marking is also found on products sold outside the EEA that have been manufactured to EEA standards. EU publications and legislative measures. 15-03-2021 Coronavirus - business continuity measures at the ERC (UPDATED 15-03-2021) 22-02-2021 ERC kicks off Horizon Europe. These tools are designed to raise the EU’s level of ambition; through the Capability Development Plan (CDP), Coordinated Annual Review on Defence (CARD), Permanent Structured Cooperation (PESCO) … It is a useful tool to find information on studying or working in the Europe. Directiva 2003/87/CE del Parlamento Europeo y del Consejo, de 13 de octubre de 2003, por la que se establece un régimen para el comercio de derechos de emisión de gases de efecto invernadero en la Comunidad y por la que se modifica la Directiva 96/61/CE del Consejo (DO L 275, 25.10.2003, pp. DisplayLogo. Call for expression of interest: EU for health security in Africa: ECDC 4 Africa CDC News-12 Apr 2021. Created in 1992, it has co-financed thousands of projects The terminology database of the European Union. Not all products must have CE marking. EU official directory. +Europa ( Più Europa, abbreviato +Eu o +E) è un partito politico italiano di orientamento europeista e liberale, nato dalla fusione fra i Radicali Italiani e il movimento Forza Europa, che si è presentato con una propria lista elettorale alle elezioni politiche italiane del 2018. European standardisation bodies If you need to involve a notified body, the CE marking must be accompanied by the identification number of the notified body. If your product is subject to several EU directives/regulations which require a CE marking to be affixed, the accompanying documents must indicate that your product conforms to all applicable EU directives/regulations. European Investment Bank; Member State level; Financing CE in practice; Education and Training; Measuring the circular economy; Toolkits and guidelines; Exchange. Discussion forum; Contribute: submit content for the website; Circular Economy Networks / Platforms; About. Search. The letters ‘CE’ appear on many products traded on the extended Single Market in the European Economic Area (EEA). The BPR aims to improve the functioning of the biocidal products market in the EU, while ensuring a high level of protection for humans and the environment. Este hecho fue llevado al Parlamento Europeo en el año 2008. Thank you for your feedback. The cost depends on which certification procedure that applies to your product and the complexity of the product etc. Welcome to Access2Markets, the new portal for EU exporters and importers! CE marking is an administrative marking that indicates conformity with health, safety, and environmental protection standards for products sold within the European Economic Area (EEA). They signify that products sold in the EEA have been assessed to meet high safety, health, and environmental protection requirements. If you are willing to give us more details, please fill in this, Licensing and selling intellectual property, Infringement of intellectual property rights, Taxes on parent companies and subsidiaries, Request a review of a public procurement procedure, E-commerce, distance and off-premises selling, Package travel and linked travel arrangements, Technical documentation and EU declaration of conformity, Classification, labelling and packaging of chemicals, conformity assessment for protective equipment, conformity assessment for 3D printing and 3D printed products to be used in a medical context, applicable legislation for leave-on hand cleaners and hand disinfectants (gel, solution), national contact points for medical devices, EN 149:2009 Respiratory protective devices – Filtering half masks to protect against particles - Requirements, testing, marking (commonly referred to as 'FFP masks'), EN 14683:2019 EN Medical face masks - Requirements and test method, EN 166:2001 Personal eye-protection – Specifications, EN 14126:2003 Protective clothing - Performance requirements and tests methods for protective clothing against infective agents, EN 14605:2009 Protective clothing against liquid chemicals - performance requirements for clothing with liquid-tight (Type 3) or spray-tight (Type 4) connections, including items providing protection to parts of the body only, EN 13795-1:2019 Surgical clothing and drapes - Requirements and test methods - Part 1: Surgical drapes and gowns, EN 13795-2:2019 Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - Part 2: Test methods, EN 455-1:2000 Medical gloves for single use - Part 1: Requirements and testing for freedom from holes (MDD), EN 455-2:2015 Medical gloves for single use - Part 2: Requirements and testing for physical properties (MMD), EN 455-3:2015 Medical gloves for single use - Part 3: Requirements and testing for biological evaluation (MDD), EN 455-4:2009 EN Medical gloves for single use - Part 4: Requirements and testing for shelf life determination (MDD), EN ISO 374-5:2017 Protective gloves against dangerous chemicals and micro-organisms - Part 5: Terminology and performance requirements for micro-organisms risks, EN ISO 13688:2013 Protective clothing - General requirements, EN ISO 10993-1:2009 Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process, EU regulation on product requirements and market surveillance, EU decision on a common framework for the marketing of products, Publications Office of the European Union, determine whether you can assess your product by yourself or if you have to involve a. EUIPO is the European Union Intellectual Property Office responsible for managing the EU trade mark and the registered Community design. We're sorry but reopeneu doesn't work properly without JavaScript enabled. As the product's manufacturer, you bear sole responsibility for declaring conformity with all requirements.