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Directive 2014/90/EU repealed Directive 96/98/EC on 18 September 2016. [ 2 ] EU Regulation 2024/1975 of 19 July 2024 layed down the rules for the application of Directive 2014/90/EU of the European Parliament and of the Council, as regards design, construction and performance requirements and testing standards for marine equipment and repealing ...
A European Union Association Agreement or simply Association Agreement (AA) is a treaty between the European Union (EU, or its predecessors), its Member States and a non-EU country or bloc of countries that governs bilateral relations. Areas frequently covered by such agreements include the development of political, trade, social, cultural and ...
Fiji – In 2023, EU and Fijian officials met to discuss potential visa-free travel for nationals of Fiji to the Schengen Area. [ 162 ] Guyana – In July 2023, Guyanese President Irfaan Ali stated that at least five EU countries had agreed to sponsor a proposal for a visa exemption for nationals of Guyana.
On 1 October 2023, the Official Journal switched to act-by-act publication. In this new production mode, the Official Journal is no longer a collation of acts with a table of contents. Instead, each act is published individually as an authentic Official Journal in PDF format. [8]
[16] [3] Josep Borrell informed EU foreign ministers that the implementation of the agreement will be "supervised by a commission from both countries and the European Union which is legally binding". [17] At a European Council summit on 23 March 2023, Borrell warned the leaders of Serbia and Kosovo that "Any attempt to question the agreement is ...
Vol. 1: Pharmaceutical legislation: medicinal products for human use. ISBN 92-828-2032-7; Vol. 2: Notice to applicants: medicinal products for human use. ISBN 0-11-975780-X; Vol. 3: Guidelines: medicinal products for human use. ISBN 92-828-2436-5; Vol. 4: Good manufacturing practices: medicinal products for human and veterinary use. ISBN 92-828 ...
EC Regulation 1223/2009 on cosmetics sets binding requirements for cosmetic products that have been made available on the market within the European Union.Manufacturers of products that fall under the category or cosmetics are required to abide by this regulation as they prepare their initial release of products and while continuing to sell said products within the Member States of the EU.
Regulation (EU) 2017/746 (IVDR) is a regulation of the European Union on the placing on the market and putting into service of in vitro diagnostic medical devices (IVD), repealing Directive 98/79/EC (IVDD), which also concerned IVD. The regulation was published in April 2017 and is closely aligned to the EU regulation on medical devices.