Esheria Regulatory Atlas
Registration, licensing, names, permits, and formal establishment requirements. These records come from release legal-2026.07.26-907 and link directly to stored legal text.
2,315 matching statutes
European Union
32017R0746
12 provisions
This Regulation sets the EU framework for in vitro diagnostic medical devices, including scope decisions, implementation by Member States, and Commission powers for certain case-by-case and urgent acts.
European Union
32026L0470
3 provisions
This segment describes changes to EU sustainability reporting and due diligence rules, including narrower reporting scope, value-chain protections, simplified third-country registration, and delegated act powers for the Commission.
European Union
32011R1178
11 provisions
This provision sets EU rules for pilot licences, medical certificates, training, examinations, records, language proficiency, and recent-experience requirements.
European Union
32024L1640
8 provisions
This segment says Member States should strengthen AML/CFT risk controls, including central registers for beneficial ownership information and stronger oversight of those registers.
European Union
32021D0085
1 provisions
The Decision says U.S. CCPs are treated as equivalent for EU purposes if they meet specified risk-management rules, and the Commission must review that basis every 3 years.
European Union
32006D0056
2 provisions
The Decision sets priorities for the European Partnership with Serbia and Montenegro, and says Serbia and Montenegro should develop a plan to address those priorities; Kosovo should have a separate plan under UN administration.
European Union
32023R2599
1 provisions
This Regulation sets rules for which shipping entity is treated as responsible and what documents and information must be given to the relevant administering authority.
European Union
32021D0038
1 provisions
This Decision sets common EU rules for end-user certificates for SALW exports and requires Member States to check, retain, and share certificate-related information.
European Union
32023R1649
1 provisions
This Regulation starts an investigation into possible circumvention of anti-dumping measures on birch plywood and requires customs authorities to register the covered imports.
European Union
32008D0210
1 provisions
The Council sets the principles, priorities, and conditions for the European Partnership with Albania, requires Albania’s competent authorities to prepare an implementation plan, and repeals Decision 2006/54/EC.
European Union
32013R0345
2 provisions
This provision sets rules for using the EuVECA label for qualifying venture capital funds and for marketing them to eligible investors.
European Union
32025D0966
1 provisions
This decision amends the annex to Decision (CFSP) 2024/2643 and takes effect on publication in the Official Journal.
European Union
32025R0965
1 provisions
This regulation amends Annex I to the earlier sanctions regulation and takes effect when published.
European Union
32005D0846
1 provisions
This Decision adds the listed persons and entity to the Annex to the related Common Position, takes effect on its adoption date, and must be published in the Official Journal.
European Union
32020R2162
1 provisions
This regulation starts an anti-dumping circumvention investigation for certain aluminium foil from Thailand and requires Member State customs to register the listed imports.
European Union
32025R0058
5 provisions
The regulation imposes a definitive anti-dumping duty on certain bus and lorry tyres from China.
European Union
32011R1083
1 provisions
This regulation amends EU restrictive-measures rules for Burma/Myanmar, including freezing listed persons’ funds and economic resources and banning making resources available to them.
European Union
32024R1915
5 provisions
This provision says the Commission is imposing a provisional anti-dumping duty on imports of mobile access equipment from China.
European Union
32025R1732
4 provisions
This provision announces a provisional anti-dumping duty on candles, tapers and similar products imported from China.
European Union
32013R1259
1 provisions
This regulation tightens EU controls on drug precursors, especially medicinal products containing ephedrine or pseudoephedrine, and adds licensing, registration, notification, monitoring, and data-processing rules.