My bookmarksSign up free
Source

Commission Implementing Regulation (EU) 2026/2096 of 18 September 2026 establishing procedures for the operation of the network for epidemiological surveillance

Commission Implementing Regulation (EU) 2026/2096 of 18 September 2026 establishing procedures for the operation of the network for epidemiological surveillance

Implementing Regulation (EU) 2026/2096 · Regulation · 8 articles

In force

Version historyWe hold this version only; in force from 2026-09-18.

Data as of 2026-10-15 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗

Procedure for membership in the dedicated networks on surveillance

Article 1

Open ↗

1.   On behalf of the national coordinating competent body of each Member State, as defined in Article 2(2) of Regulation (EC) No 851/2004, the national coordinator shall designate members in the dedicated networks on surveillance (‘dedicated networks’). That membership shall be revoked if a network member moves into a new professional role outside the disease, related special health issue or public health function remit of the network. 2.   The designations provided for in paragraph 1 shall be: (a) made electronically, through the dedicated stakeholder relationship management platform hosted by the ECDC; (b) specific as to the specific role of the network member as a national focal point or operational contact point, and specific as to the dedicated network regarding disease, related special health issue or public health function. 3.   The national coordinating competent body may also designate alternates to act as substitutes in the absence of the primary network members. 4.   If no members are designated for a given dedicated network, all relevant surveillance interactions with the ECDC shall be channelled through the national coordinator.

National focal points

Article 2

Open ↗

National focal points shall, each within their dedicated network: (a) oversee any exchange of surveillance data or surveillance-related information between their Member State and the ECDC; (b) advise their national coordinator on the designation of operational contact points and participants in network and other relevant meetings; (c) provide scientific and technical advice to the ECDC; (d) ensure submission of timely, complete and accurate national surveillance data and any other information relevant to surveillance to EpiPulse within the deadlines set by the ECDC after consulting the dedicated network; (e) coordinate activities with other network members appointed by the same coordinating competent body and with relevant national actors as well as with relevant partners, including the EU Reference Laboratories for public health, and collaborate closely with their counterparts in the other Member States.

Operational contact points

Article 3

Open ↗

Operational contact points shall, each within their dedicated network: (a) be the main contact for any exchange of surveillance data or surveillance-related information between their Member State and the ECDC; (b) submit timely, complete and accurate national surveillance data to EpiPulse within the deadlines set by the ECDC after consulting the dedicated networks; (c) review draft surveillance outputs produced by the ECDC and contribute to the interpretation of surveillance results alongside the ECDC and the other operational contact points; (d) inform the ECDC about national data sources and surveillance systems; (e) oversee the implementation of surveillance metadata changes at national level; (f) coordinate activities with other network members appointed by the same coordinating competent body and relevant national actors as well as with relevant partners, including the EU reference laboratories for public health, and collaborate closely with their counterparts in the other Member States.

The ECDC secretariat

Article 4

Open ↗

The ECDC shall: (a) be the coordination and communication hub for all activities of the dedicated networks and provide the scientific secretariat and administrative support; (b) provide: (i) the dedicated stakeholder relationship management platform and relevant instructions for the designation of network members and updating of their membership status; (ii) technical surveillance support and foster technical and scientific collaboration within and across the dedicated networks; (c) organise regular network meetings to share data and best practices, highlight data quality issues and other surveillance shortcomings and discuss strategic choices within and across the dedicated networks; (d) liaise with relevant partners, including the EU reference laboratories for public health, the World Health Organization (‘WHO’), other EU agencies, on behalf of the dedicated networks to coordinate activities (including on One Health), share data, facilitate cooperation or reduce Member State burden, as appropriate.

Technical work procedures

Article 5

Open ↗

1.   The ECDC shall announce the start and end of each annual routine surveillance data collection to the dedicated networks and share with each of them the latest version of the relevant reporting protocol with the disease-specific common data structure. 2.   The operational contact points of the dedicated networks shall submit their national surveillance data electronically to EpiPulse in compliance with the reporting deadline set by the ECDC after consulting the dedicated network and with the common data structure referred to in paragraph 1. 3.   The operational contact points of the disease networks shall review the automated data validation report in EpiPulse and any additional validation feedback from the ECDC and, where applicable, resubmit data at the level of quality required to reach the surveillance objectives. 4.   The ECDC shall analyse and communicate the routine surveillance data in a timely manner and at least at the frequency of data collection.

Administrative procedures

Article 6

Open ↗

1.   The ECDC may appoint a coordination committee to facilitate communication between the ECDC and a given dedicated network. 2.   The ECDC shall convene regular network meetings to discuss surveillance objectives, case definitions, metadata changes, data analysis plans, surveillance findings, best practices or technical innovations in consultation with the relevant network coordination committee, if appointed. 3.   Network meetings may be held in person, online or in hybrid format, and the ECDC shall provide the secretariat. 4.   The ECDC shall share a final agenda with the network no later than one week before the meeting. The ECDC shall take minutes and share a meeting report with all participants. It shall follow up on any matters requiring further action in consultation with the network coordination committee, if appointed, and report back to the network in writing or at the following network meeting. 5.   When network meetings are held online or in hybrid format, the ECDC may invite written comments on proposals. For any urgent technical discussion between network meetings, the ECDC may consult the relevant network coordination committee, if appointed, in writing or through online means. 6.   The ECDC shall disseminate any documents for network or coordination committee meetings and consultations well in advance and leave sufficient time for thorough review and internal coordination of national positions and written opinions by the national coordinating competent body. 7.   For surveillance schemes run jointly with the WHO, network meetings may be held jointly, with the ECDC and the WHO collaborating in organising these meetings and with cost arrangements to be agreed between the ECDC and the WHO.

Periodic evaluation

Article 7

Open ↗

The ECDC and the dedicated networks shall periodically evaluate the procedures for the operation of the network for epidemiological surveillance and inform the Commission about the outcome of those evaluations.

Entry into force

Article 8

Open ↗

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

Other acts of the same type
Commission Implementing Regulation (EU) 2022/965 of 21 June 2022 authorising the placing on the market of kernels from the edible variety of Jatropha curcas L. as a novel food and amending Implementing Regulation (EU) 2017/2470 (Text with EEA relevance)Commission Implementing Regulation (EU) 2022/966 of 21 June 2022 amending Implementing Regulation (EU) 2017/2470 as regards the conditions of use, the specific labelling requirements and specifications of the novel food Calanus finmarchicus oil (Text with EEA relevance)Council Implementing Regulation (EU) 2022/949 of 20 June 2022 implementing Regulation (EU) 2016/1686 imposing additional restrictive measures directed against ISIL (Da’esh) and Al-Qaeda and natural and legal persons, entities or bodies associated with themCommission Implementing Regulation (EU) 2022/960 of 20 June 2022 correcting the Czech language version of Implementing Regulation (EU) 2015/1502 on setting out minimum technical specifications and procedures for assurance levels for electronic identification means pursuant to Article 8(3) of Regulation (EU) No 910/2014 of the European Parliament and of the Council on electronic identification and trust services for electronic transactions in the internal market (Text with EEA relevance)Commission Implementing Regulation (EU) 2022/961 of 20 June 2022 authorising the placing on the market of tetrahydrocurcuminoids as a novel food and amending Implementing Regulation (EU) 2017/2470 (Text with EEA relevance)Commission Delegated Regulation (EU) 2022/2236 of 20 June 2022 amending Annexes I, II, IV and V to Regulation (EU) 2018/858 of the European Parliament and of the Council as regards the technical requirements for vehicles produced in unlimited series, vehicles produced in small series, fully automated vehicles produced in small series and special purpose vehicles, and as regards software update (Text with EEA relevance)Commission Implementing Regulation (EU) 2022/2581 of 20 June 2022 laying down implementing technical standards for the application of Directive 2013/36/EU of the European Parliament and of the Council with regard to provision of information in applications for authorisation of a credit institution (Text with EEA relevance)Commission Regulation (EU) 2022/943 of 17 June 2022 correcting certain language versions of Annex I to Regulation (EC) No 2195/2002 of the European Parliament and of the Council on the Common Procurement Vocabulary (CPV) (Text with EEA relevance)Commission Implementing Regulation (EU) 2022/944 of 17 June 2022 laying down rules for the application of Regulation (EU) 2017/746 of the European Parliament and of the Council as regards the tasks of and criteria for European Union reference laboratories in the field of in vitro diagnostic medical devices (Text with EEA relevance)Commission Implementing Regulation (EU) 2022/945 of 17 June 2022 laying down rules for the application of Regulation (EU) 2017/746 of the European Parliament and the Council with regard to fees that may be levied by EU reference laboratories in the field of in vitro diagnostic medical devices (Text with EEA relevance)Council Regulation (EU) 2022/972 of 17 June 2022 amending Regulation (EU) 2021/2283 opening and providing for the management of autonomous tariff quotas of the Union for certain agricultural and industrial productsCouncil Regulation (EU) 2022/1008 of 17 June 2022 amending Regulation (EU) 2021/2278 suspending the Common Customs Tariff duties referred to in Article 56(2), point (c), of Regulation (EU) No 952/2013 on certain agricultural and industrial products

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

Contents

What to look at next