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Лого на Европейската комисия
Food Safety

Information on the procedure for the renewal of existing authorisations for smoke flavourings

Regulation (EC) No 2065/2003 establishes a procedure for the safety assessment and the authorisation of smoke flavouring primary products with a view to ensuring a high level of protection of human health and the interests of consumers and the effective functioning of the internal market. That Regulation provides that smoke flavourings or food containing them may not be placed on the market if a smoke flavouring that is not an authorised primary product is present.

Commission Implementing Regulation (EU) No 1321/2013 authorised 10 smoke flavouring primary products for a 10-year period, due to expire on 1 January 2024.

As per Article 12(1) of Regulation (EC) No 2065/2003, authorisation holders wishing to renew the authorisations must submit applications at the latest 18 months before the expiry date of the authorisation. The applications shall be submitted through the E-submission Food Chain platform.

In light of the upcoming deadline for requesting such renewals, the Commission services wish to provide authorisation holders and other interested parties with the following information in respect of this process.

Authorisation holder

In accordance with Article 12(1) of Regulation (EC) No 2065/2003, only the actual authorisation holders may request the said renewal of authorisation.

Insofar as the ownership of an authorisation would have changed or if changes would be intended in the near future, it is important that authorisation holders take this element into account, so as not to compromise a possible application for renewal of an existing authorisation. The change of authorisation holder can be requested by means of an application for modification of the existing authorisation by the authorisation holder itself.

Requirements arising from Regulation (EU) 2019/1381

The provisions of Regulation (EU) 2019/1381 apply to all applications under Union Food law submitted on or after 27 March 2021 (see Article 10)  and that this Regulation amended in particular the General Food Law and Regulation (EC) No 2065/2003 as regards certain provisions that are relevant for the applications for renewal of authorisations of smoke flavouring primary products. In particular:

  • Article 32a of the General Food Law, which allows potential applicants to request the European Food Safety Authority ('the Authority') for advice on the rules applicable to, and the content required for, an application for which Union law foresees the delivery of a scientific output by the Authority.
  • Article 32b of the General Food Law, which requires business operators and laboratories and other testing facilities located in the Union to notify the Authority of the title and scope of any study commissioned or carried out to support an application. Non-compliance with these requirements may lead to procedural consequences for the application, including its possible inadmissibility or invalidity, as set out by Article 32b(4) and (5) of the General Food Law.
  • Article 32c(1) of the General Food Law, which allows potential applicants for renewal of authorisations to notify the Authority of intended studies with a view to obtaining the Authority's advice on the content of the intended renewal application, as well as on the design of the studies.
  • Articles 14 and 15 of Regulation (EC) No 2065/2003, which in turn refer to the proactive disclosure and confidentiality requirements set out respectively in Articles 38 and 39 to 39e of the General Food Law. As a result, information, studies and data supporting applications submitted on, or as of, 27 March 2021 to the Authority are made publicly available by it unless a confidentiality request has been submitted pursuant to the Authority's Practical Arrangements concerning Transparency and Confidentiality.
  • Article 32c(2) of the General Food Law also provides for a consultation of the public and of stakeholders on the basis of the non-confidential version of the application, immediately after it is made public in accordance with Articles 38 to 39e of the General Food Law.

Applicants are invited to refer to the General Food Law and Regulation (EC) No 2065/2003 as well as to the Authority's Practical Arrangements.

Procedure for the renewal of authorisations

Deadline for applications for the renewal of authorisations

Authorisation holders must request the renewal of authorisations for smoke flavouring primary products at the latest 18 months before the expiry date of the authorisation. This deadline is applicable in respect of the authorisations that are presently included in the Union list of authorised smoke flavouring primary products and which are due to expire on 1 January 2024.

Handling of applications for the renewal of authorisations

In accordance with Article 8(3)(a) of Regulation (EC) No 2065/2003, the Authority shall verify that the application is valid in the sense that it contains the information referred to in Article 7(3) of the Regulation, which refers to Annex II, listing the information necessary for the scientific evaluation of primary products, including point 6 concerning toxicological data. This information should be compiled in accordance with Scientific Guidance for the preparation of applications on smoke flavouring primary products and the Administrative guidance for the preparation of applications on smoke flavouring primary products.

Applicants may deviate from the Authority's guidance documents and submit alternative toxicological studies to the ones recommended by the Authority, provided that they can justify their strategy and that the submitted alternative data could address the safety endpoints as indicated in the guidance, allowing to assess the safety of the smoke flavouring primary product under the proposed conditions of use.

Account may be  given to the fact that it might not have been feasible to complete the Extended One Generation Reproductive Toxicity study (EOGRTS), conducted according to OECD TG 443 as recommended by the Authority in the scientific guidance, or an alternative toxicological study to the EOGRTS, during the period between the publication of the Authority's guidance documents and the deadline for applying for the renewal of the existing of authorisations for smoke flavouring primary products.

In this context, the Authority could confirm validity of the renewal applications without the complete data required in the Authority's scientific guidance provided the application contains:

  • Complete dataset, regarding the characterisation of the smoke flavouring primary product, its genotoxicity and exposure data;
  • Information demonstrating that the EOGRTS (or an alternative toxicological study to the EOGRTS) is ongoing by providing:
    • a statement from the applicant detailing the reasons for not providing the EOGRTS (or the alternative toxicological study) and a declaration that the study has been already commissioned to a contract research laboratory (CRO);
    • a notification of the EOGRTS (or the alternative toxicological study) in the Authority's database for study notifications,  referred to in Article 32b of Regulation (EC) No 178/2002, i.e. the Transparency Regulation. The notification of the study has to be performed by the applicant after the commissioning of the study and before its starting date. Moreover, this notification must be carried out before submitting the renewal application to the Commission.

Upon validation, the Authority will make publicly available the non-confidential version of the application as submitted by the applicant.

A second, non-confidential version of the application dossier implementing the Authority’s confidentiality decision may be disclosed by the Authority later during the safety assessment in case the Authority disagrees with one or more of the confidentiality requests submitted by the applicant.

The Authority will first evaluate the available full dataset submitted at the time of application (chemical characterisation, genotoxicity data, dietary exposure) with the aim of ruling out potential concern with respect to genotoxicity by the end of September 2023. Second, provided that the genotoxic concern can be ruled out, the Authority will proceed to complete the rest of the safety assessment, in particular after receiving the submission of the final EOGRTS (or the alternative toxicological study) for the concerned applications for the renewal of authorisations for smoke flavouring primary product.

Procedure in case of delays of the renewal procedure for reasons beyond the control of the authorisation holder

In accordance with Article 12(4) of Regulation (EC) No 2065/2003, where no decision is taken on the concerned application for reasons beyond the control of the authorisation holder, the period of authorisation of products for which a procedure of renewal is ongoing would be extended by six months. Where this provision is applied, the Commission would inform the authorisation holder and the Member States about the delay.

This provision seeks to ensure that the procedure for the renewal of authorised smoke flavouring primary products can be completed without leading to disruptions on this regulated market. Taking this into account as well as the need to ensure that time-pressure would not prevent the Authority and the Commission to carry out the thorough safety assessment and the risk management decisions that are necessary to protect human health and the interests of consumers, the Commission considers that, as long as the conditions of Article 12(4) would be complied with, multiple extensions may occur for a given application for renewal.

The application of this provision is subject to the condition that it can be established that the absence of a decision on the renewal of an authorisation is due to 'reasons beyond the control of the authorisation holder'.

To ensure that the conditions for the extension provided for in Article 12(4) are met, the applicants are invited to report to the Commission every 6 months on the situation of their application and on the status of the data being generated. Such reporting should be carried out by the end of the months of May and November and addressed to the Commission services at the following address: SANTE-SMOKE-FLAVOURINGS@ec.europa.eu including the Authority’s address in copy: FDP@efsa.europa.eu.

Kindly note that this information is intended to assist authorisation holders in the application of Regulation (EC) No 2065/2003 as regards possible applications for renewal of authorisations for smoke flavouring primary products but that only the Court of Justice of the European Union is competent to authoritatively interpret Union law.