My bookmarksSign up free
Source

Commission Implementing Regulation (EU) 2021/2071 of 25 November 2021 subjecting certain vaccines and active substances used for the manufacture of such vaccines to export surveillance

Commission Implementing Regulation (EU) 2021/2071 of 25 November 2021 subjecting certain vaccines and active substances used for the manufacture of such vaccines to export surveillance

Implementing Regulation (EU) 2021/2071 · Regulation · 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 ↗

Article 1

Open ↗

1.   The following goods shall be subject to export surveillance for a period of 24 months from the date of entry into force of this Regulation: (a) vaccines against SARS-related coronaviruses (SARS-CoV species) currently falling under CN code 3002 20 10, irrespective of their packaging; (b) active substances, including master and working cell banks used for the manufacture of such vaccines, currently falling under CN codes ex 2933 99 80, ex 2934 99 90, ex 3002 90 90 and ex 3504 00 90. 2.   For the purposes of this Regulation, ‘export’ means: (a) an export of Union goods under the export procedure within the meaning of Article 269(1) of Regulation (EU) No 952/2013; (b) a re-export of non-Union goods within the meaning of Article 270(1) of that Regulation after such goods have been subject to manufacturing operations including filling and packaging within the customs territory of the Union.

Article 2

Open ↗

The export or re-export declaration of the goods mentioned in Article 1 shall, during the time referred to therein, include the TARIC additional codes mentioned in the Annex, or any corresponding future codes, and shall indicate the number of doses (in case of multi-dose containers, the number of doses for adults).

Article 3

Open ↗

The Commission shall make the information on the exports publicly available, due account being taken of the confidentiality of the data.

Supplementary provisions

TARIC ADDITIONAL CODES

ANNEXSupplementary provisions

Open ↗

ANNEX TARIC ADDITIONAL CODES Manufacturer Taric additional code for vaccines against SARS-related coronaviruses (SARS-CoV species) Taric additional code for active substances  ( *1 ) AstraZeneca AB 4500 4520 Pfizer / BioNTech 4501 4521 Moderna Switzerland / Moderna Inc 4502 4522 Janssen Pharmaceutica NV 4503 4523 CureVac AG 4504 4524 Sanofi Pasteur / GlaxoSmithKline Biologicals S.A 4505 4525 Novavax 4506 4526 Valneva 4507 4527 Gedeon Richter 4508 4528 Arcturus 4509 4529 PCI Pharma 4510 4530 Other manufacturers 4999 4999 Company TARIC additional code for other substances  ( *2 ) All manufacturers 4599 ( *1 )   active substances including master and working cell banks used for the manufacture of vaccines against SARS-related coronaviruses (SARS-CoV species). ( *2 )    ‘Other substances’ are products or substances that are not going to be used to manufacture vaccines against SARS-related coronaviruses (SARS-CoV species), but that are classified under the same CN codes as the active substances.

Other acts of the same type
Commission Implementing Regulation (EU) 2025/2275 of 4 November 2025 on the registration of the geographical indication Miel de tilleul de Picardie (PGI) in the Union register of geographical indications pursuant to Regulation (EU) 2024/1143 of the European Parliament and of the CouncilCommission Implementing Regulation (EU) 2025/2219 of 3 November 2025 imposing provisional anti-dumping duties on imports of softwood plywood originating in the Federative Republic of BrazilCommission Implementing Regulation (EU) 2025/2220 of 3 November 2025 amending Annex XVI to Implementing Regulation (EU) 2021/404 as regards the entry for North Macedonia in the list of third countries or territories or zones thereof authorised for the entry into the Union of consignments of casingsCommission Implementing Regulation (EU) 2025/2231 of 3 November 2025 amending Implementing Regulation (EU) 2020/1201 as regards the list of infected zones for containment of Xylella fastidiosa (Wells et al.)Commission Delegated Regulation (EU) 2026/117 of 3 November 2025 amending Regulation (EU) 2022/2343 of the European Parliament and of the Council laying down management, conservation and control measures applicable in the Indian Ocean Tuna Commission (IOTC) Area of Competence, amending Council Regulations (EC) No 1936/2001, (EC) No 1984/2003 and (EC) No 520/2007Commission Implementing Regulation (EU) 2025/2203 of 31 October 2025 amending Implementing Regulation (EU) 2023/564 as regards the transfer into electronic format of the records of plant protection products kept by professional usersCommission Implementing Regulation (EU) 2025/2210 of 31 October 2025 laying down rules for the application of Regulation (EU) 2023/956 of the European Parliament and of the Council as regards goods and processed products brought to the continental shelf or the exclusive economic zone of Member StatesCommission Implementing Regulation (EU) 2025/2215 of 31 October 2025 amending Implementing Regulation (EU) 2022/964 as regards administrative changes to the Union authorisation for the biocidal product family SOPUROXIDCommission Implementing Regulation (EU) 2025/2218 of 31 October 2025 amending Implementing Regulation (EU) 2023/402 as regards administrative changes to the Union authorisation of the biocidal product family CMIT/MIT SOLVENT BASED and correcting that RegulationCommission Implementing Regulation (EU) 2025/2221 of 31 October 2025 amending Implementing Regulation (EU) 2023/364 as regards administrative changes to the Union authorisation of the biocidal product family IPA Family 1Commission Implementing Regulation (EU) 2025/2171 of 29 October 2025 concerning the renewal of the authorisation of calcium D-pantothenate (vitamin B5) and D-panthenol (vitamin B5) as feed additives for all animal species and repealing Implementing Regulation (EU) No 669/2014Commission Implementing Regulation (EU) 2025/2172 of 29 October 2025 granting protection in the Union to the Geographical Indication Vaj Ulliri Valmi Elbasan registered in the International Register of Appellations of Origin and Geographical Indications of the Geneva Act

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

Contents

What to look at next