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English: Commission Regulation (EU) No 722-2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90-385-EEC and 93-42-EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin (Text with EEA relevance)
Directive 2009/49/EC of the European Parliament and of the Council amending Council Directives 78/660/EEC and 83/349/EEC as regards certain disclosure requirements for medium-sized companies and the obligation to draw up consolidated accounts, 18 June 2009, intended to reduce the administrative burdens placed on businesses. Implementation was ...
The Medical Device Directive—Council Directive 93/42/EEC of 14 June 1993 concerning medical devices—is intended to harmonise the laws relating to medical devices within the European Union. The MD Directive is a 'New Approach' Directive and consequently in order for a manufacturer to legally place a medical device on the European market the ...
If a member state fails to pass the required national legislation, or if the national legislation does not adequately comply with the requirements of the directive, the European Commission may initiate legal action against the member state in the European Court of Justice. This may also happen when a member state has transposed a directive in ...
Council Directive of 23 July 1990 on the common system of taxation applicable to mergers, divisions, partial divisions, transfers of assets and exchanges of shares concerning companies of different Member States and to the transfer of the registered office, of an SE or SCE, between Member States (90-434-EEC) (repealed)
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Commission Directive 90-630-EEC of 30 October 1990 adapting to technical progress Council Directive 77-649-EEC on the approximation of the laws of the Member States relating to the field of vision of motor vehicle drivers ( ) Title
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