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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
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 “Valbazen 100 mg/ml Total Spectrum Wormer oral suspension and associated names, including its generic/hybrid products “ containing the active substance “Albendazole”
Commission Regulation (EU) …/… of XXX amending Annexes II, III and IV to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for aclonifen, acrinathrin, Bacillus pumilus QST 2808, chlorantraniliprole, ethirimol, lufenuron, penthiopyrad, picloram and Pseudomonas sp. strain DSMZ 13134 in or on certain products
Commission Implementing Regulation (EU) …/… of XXX amending Annexes II, III and V to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for clethodim, dazomet, hexythiazox, metam and sethoxydim in or on certain products
Commission Implementing Decision .../... of XXX establishing a list of geographical indications protected under Regulation (EU) 2019/787 of the European Parliament and of the Council to be filed as applications for international registration pursuant to Article 2 of Regulation (EU) 2019/1753 of the European Parliament and of the Council
Commission Implementing Decision of XXX concerning the extension of the action taken by the Croatian Ministry of Health permitting the making available on the market and use of the biocidal product Biobor JF in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council
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 “Modified live porcine respiratory and reproductive syndrome (PRRS) virus vaccines“ containing “Porcine respiratory and reproductive syndrome virus vaccine (live)”
Commission Implementing Decision .../... of XXX granting an authorisation under Regulation (EC) No 1907/2006 of the European Parliament and of the Council to BioMarin International Limited for certain uses of 4-(1,1,3,3-tetramethylbutyl)phenol, ethoxylated (4-tert-OPnEO)
Proposal for a Regulation of the European Parliament and of the Council laying down harmonised conditions for the marketing of construction products, amending Regulation (EU) 2019/1020 and repealing Regulation (EU) 305/2011

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