My bookmarksSign up free
Source

Council Implementing Decision (EU) 2025/2628 of 18 December 2025 on the Union Resettlement and Humanitarian Admission Plan (2026-2027)

Council Implementing Decision (EU) 2025/2628 of 18 December 2025 on the Union Resettlement and Humanitarian Admission Plan (2026-2027)

Implementing Decision (EU) 2025/2628 · Decision · 5 articles

Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗

The Union contribution to the Global Resettlement Needs (2026-2027)

Article 1

Open ↗

1.   The total number of third-country nationals or stateless persons to be admitted to the territory of the Member States under the Union Resettlement and Humanitarian Admission Plan (the ‘Union Plan’) during the implementing period (2026-2027) is up to 10 430. 2.   The participation of the Member States and their contributions to the total number of persons to be admitted and the proportion of the persons who are to be subject to resettlement, to humanitarian admission and to emergency admission are laid down in the Annex to this Decision.

Specifications of the regions from which resettlement and humanitarian admission are to take place

Article 2

Open ↗

Admissions to the territory of the Member States under the Union Plan shall occur from: (a) countries along the main migratory routes leading to the Union through the Mediterranean and Atlantic routes, with a view to providing access to safe and legal pathways in key transit regions to those in need of protection, to supporting the implementation of a whole-route approach, and to contributing to those countries’ capacity, including by improving reception and international protection conditions; (b) countries in the Americas, with a particular focus on Central and Latin America, in particular in the light of the socio-cultural ties that might foster the integration of those admitted into the Union in line with the Union Plan; (c) countries with which the Union or its Member States have established a cooperative dialogue or are progressing towards the achievement of broader migration management and international protection objectives.

Monitoring and data collection

Article 3

Open ↗

1.   In order to facilitate monitoring as regards the implementation of their voluntary contributions, when providing the necessary information to the Commission and the Agency pursuant Regulation (EU) 2024/1350 for the purpose of drawing up the Commission’s report on the application of that Regulation, Member States specify, in particular: (a) the number of third-country nationals or stateless persons admitted by the Member States in line with the Union Plan during the reference period; (b) a specification of the type of admission (resettlement, humanitarian admission or emergency admission); (c) a specification of the non-EU country from which admissions occurred. 2.   Data and information collected on a regular basis by the Commission and the Agency shall be based on a common framework and indicators.

Entry into force

Article 4

Open ↗

This Decision shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .

Supplementary provisions

ANNEXSupplementary provisions

Open ↗

ANNEX Member States’ contributions to the Union Resettlement and Humanitarian Admission Plan (2026-2027)   Resettlement Humanitarian admission Emergency admission  ( *1 ) Total Bulgaria 120   Up to 20 120 France 1 200     1 200 Ireland 1 200 100   1 300 Italy 800 2 000   2 800 Malta 10     10 Netherlands 1 400   Up to 40 1 400 Romania 300     300 Spain 2 400     2 400 Sweden 900     900 Total 8 330 2 100   10 430 ( *1 )   Counted within the contributions for resettlement

Other acts of the same type
Commission Implementing Decision (EU) 2025/945 of 22 May 2025 postponing the expiry date of the approval of nonanoic acid for use in biocidal products of product-type 2 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the CouncilCommission Implementing Decision (EU) 2025/946 of 22 May 2025 postponing the expiry date of the approval of octanoic acid for use in biocidal products of product-type 4 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the CouncilCommission Implementing Decision (EU) 2025/947 of 22 May 2025 postponing the expiry date of the approval of iodine for use in biocidal products of product-type 3 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the CouncilCommission Implementing Decision (EU) 2025/949 of 22 May 2025 postponing the expiry date of the approval of decanoic acid for use in biocidal products of product-type 4 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the CouncilCommission Implementing Decision (EU) 2025/950 of 22 May 2025 postponing the expiry date of the approval of 1R-trans phenothrin for use in biocidal products of product-type 18 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the CouncilCommission Implementing Decision (EU) 2025/951 of 22 May 2025 postponing the expiry date of the approval of polyvinylpyrrolidone iodine for use in biocidal products of product-types 1 and 3 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the CouncilCommission Implementing Decision (EU) 2025/952 of 22 May 2025 postponing the expiry date of the approval of S-methoprene for use in biocidal products of product-type 18 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the CouncilCommission Implementing Decision (EU) 2025/970 of 22 May 2025 postponing the expiry date of the approval of IPBC for use in biocidal products of product-type 8 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the CouncilCommission Implementing Decision (EU) 2025/998 of 22 May 2025 postponing the expiry date of the approval of bis(N-cyclohexyl-diazenium-dioxy)-copper (Cu-HDO) for use in biocidal products of product-type 8 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the CouncilCommission Implementing Decision (EU) 2025/1083 of 22 May 2025 amending Implementing Decision (EU) 2024/2207 concerning certain emergency measures relating to sheep pox and goat pox in Greece (notified under document C(2025) 3430)Commission Implementing Decision (EU) 2025/1089 of 22 May 2025 amending the Annex to Implementing Decision (EU) 2023/2447 concerning emergency measures in relation to outbreaks of highly pathogenic avian influenza in certain Member States (notified under document C(2025) 3429)Council Decision (Euratom) 2025/1134 of 22 May 2025 on the adoption of the 2024-2027 high flux reactor supplementary research programme at Petten to be implemented by the Joint Research Centre for the European Atomic Energy Community

Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.

Contents

What to look at next