Go to basic regulation, all versions and amendments of REACH in EUR-Lex.


Passenger rights Passenger rights and coronavirus. Eine Verordnung der Europäischen Union (englisch regulation, Kurzform „Verordnung (EU)“, umgangssprachlich EU-Verordnung) ist ein Rechtsakt der Europäischen Union mit allgemeiner Gültigkeit und unmittelbarer Wirksamkeit in den Mitgliedstaaten. Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006. REGULATION (EC) No . The treaties (primary legislation) are the basis or ground rules for all EU action. Die Richtlinie 98/79/EG über In-vitro-Diagnostika (IVD) wird nicht in der Medizinprodukte-Verordnung aufgehen, sondern durch die eigene neue Verordnung … New EU trade mark regulation Changes applying 1 October 2017 On 23 March 2016, Regulation (EU) 2015/2424 of the European Parliament and the Council amending the Community trade mark regulation (the Amending Regulation) entered into force. EU legislation is divided into primary and secondary. Die Verordnung (EU) 2017/745 über Medizinprodukte löst die Medizinprodukte-Richtlinien (Richtlinie 93/42/EWG über Medizinprodukte (MDD), Richtlinie 90/385/EWG aktive implantierbare Medizinprodukte (Active Implantable Medical Devices – AIMD)) ab. On this page you will find the regulations that govern the EU trade mark system as well as the EU directive approximating the laws of the EU … Secondary legislation – which includes regulations, directives and decisions – are derived from the principles and objectives set out in the treaties. On this page you will find the regulations that govern the EU trade mark system as well as the EU directive approximating the laws of the EU … The treaties (primary legislation) … Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance. If you are a manufacturer, authorised representative, importer or distributor of medical devices in the EU, or a regulatory affairs or quality management professional involved with medical devices, you need to know how to comply. Regulations can be distinguished from directives which, at least in principle, need to be transposed into national law. A regulation is a legal act of the European Union that becomes immediately enforceable as law in all member states simultaneously. Medical Devices Regulation: Commission welcomes Council support to prioritise the fight against coronavirus ( 22.04.2020 ) The European Commission welcomes the adoption by the European Parliament and the Council of the proposal to postpone by one year the date of application of the Medical Devices Regulation. New EU trade mark regulation Changes applying 1 October 2017 On 23 March 2016, Regulation (EU) 2015/2424 of the European Parliament and the Council amending the Community trade mark regulation (the Amending Regulation) entered into force. As an air, rail, ship or bus passenger, you have rights when travelling in the EU.. More on: EU legislation on passenger rights is designed to ensure that, irrespective of the type of transport, passengers are guaranteed the same, minimum level of protection wherever they are in the EU. 1223/2009 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 30 November 2009. on cosmetic products (recast) (Text with EEA relevance) THE EUROPEAN PARLIAMENT AND THE COUNCIL OF THE EURO­ PEAN UNION, Having regard to the Treaty establishing the European Commu­ nity, and in particular Article 95 thereof,