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Commission Implementing Decision of XXX granting an authorisation for a use of dibutyl phthalate (DBP) under Regulation (EC) No 1907/2006 of the European Parliament and of the Council
Draft Commission Implementing Decision of XXX concerning, in the framework of Article 13 of Commission Regulation (EC) No 1234/2008, the marketing authorisations for medicinal products for veterinary use "Resflor solution injectable and associated names", which contain the active substances "Florfenicol and Flunixin"
Draft Commission Implementing Decision of XXX concerning, in the framework of Article 35 of Directive 2001/82/EC of the European Parliament and of the Council, the marketing authorisations for " Suanovil 20 and associated names, Captalin and associated names and generic products thereof ", veterinary medicinal products which contain the active substance " spiramycin "
Draft Commission Implementing Decision granting marketing authorisation under Regulation (EC) No 726/2004 of the European Parliament and of the Council for "Bovela", a veterinary medicinal product
Commission Implementing Decision of XXX amending, pursuant to the annual review, Decision C(2011)2785(final) granting in exceptional circumstances marketing authorisation for "BLUEVAC BTV8 - Bluetongue virus inactivated, serotype 8", a veterinary medicinal product
Proposal for a Regulation of the European Parliament and of the Council amending Regulation (EC) No 1829/2003 as regards the possibility for the Member States to restrict or prohibit the use of genetically modified food and feed on their territory
Commission Implementing Decision of XXX establishing a common format for the submission of Member State reports on the implementation of Directive 2004/42/EC of the European Parliament and of the Council on the limitation of emissions of volatile organic compounds due to the use of organic solvents in certain paints and varnishes and vehicle refinishing products
Commission Implementing Decision of XXX granting an authorisation for some uses of trichloroethylene under Regulation (EC) No 1907/2006 of the European Parliament and of the Council
Commission Implementing Decision of XXX concerning, in the framework of Article 107e of Directive 2001/83/EC of the European Parliament and of the Council, the marketing authorisations of medicinal products for human use which contain the active substance "Orlistat"
Proposal for a Regulation of the European Parliament and of the Council amending Council Regulation (EC) No 768/2005 establishing a Community Fisheries Control Agency
Commission Implementing Decision authorising the placing on the market of trans-resveratrol as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council
Commission Implementing Decision authorising the placing on the market of organic silicon (monomethylsilanetriol) as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council
Commission Recommendation of XXX on a coordinated control plan on the official control of certain foods marketed through the Internet
Commission Implementing Decision on a derogation from mutual recognition of the authorisation of biocidal products containing creosote by France in accordance with Article 37 of Regulation (EU) No 528/2012 of the European Parliament and of the Council
Commission Implementing Decision of XXX concerning, in the framework of Article 107i of Directive 2001/83/EC of the European Parliament and of the Council, the marketing authorisations of medicinal products for human use which contain the active substance “hydroxyethyl starch (HES), solutions for infusion”
Commission implementing decision on the publication of the reference of the harmonised standard EN 1621-4:2013 on “Motorcyclists' protective clothing against mechanical impact - Part 4: Motorcyclists' inflatable protectors - Requirements and test methods” pursuant to Regulation (EU) No 1025/2012 of the European Parliament and of the Council
Commission Recommendation (EU) 2019/794 of 15 May 2019 on a coordinated control plan with a view to establishing the prevalence of certain substances migrating from materials and articles intended to come into contact with food
Commission Implementing Decision concerning, in the framework of Article 31 of Directive 2001/83/EC of the European Parliament and of the Council, the marketing authorisations of medicinal products for human use which contain the active substance "methocarbamol/paracetamol 380 mg/300 mg"
Commission Implementing Decision of XXX concerning, in the framework of Article 31 of Directive 2001/83/EC of the European Parliament and of the Council, the marketing authorisations of fosfomycin-containing medicinal products for human use which contain one or more of the active substances "fosfomycin calcium, fosfomycin disodium, fosfomycin sodium and fosfomycin trometamol"
Commission Regulation .../... amending Regulation (EC) No 1881/2006 as regards maximum levels of acrylamide in certain foodstuffs for infants and young children
Commission Implementing Decision …/... concerning, in the framework of Article 107e of Directive 2001/83/EC of the European Parliament and of the Council, the marketing authorisations of medicinal products for human use which contain the active substance " midazolam (oromucosal solution, treatment of prolonged, acute, convulsive seizures)"
Commission Implementing Decision .../... partially granting an authorisation for certain uses of chromium trioxide under Regulation (EC) No 1907/2006 of the European Parliament and of the Council (REACHLaw Ltd)
Commission Implementing Decision .../... of XXX concerning, in the framework of Article 29 of Directive 2001/83/EC of the European Parliament and of the Council, the marketing authorisations for “Ibuprofen Kabi 400 mg Infusionslösung and associated names”, medicinal products for human use which contain the active substance “ibuprofen” "
Commission Implementing Decision .../... concerning, in the framework of Article 35 of Directive 2001/82/EC of the European Parliament and of the Council, the marketing authorisations for veterinary medicinal products containing stresnil 40 mg/ml solution for injection for pigs and associated names, and generic products thereof
Commission Implementing Decision of XXX concerning, in the framework of Article 35 of Directive 2001/82/EC of the European Parliament and of the Council, the marketing authorisations for veterinary medicinal products containing tiamulin hydrogen fumarate presented as premix for medicated feeding stuff and oral powder for in-feed use to be administered to pigs

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