Consultation on applications for authorisation of miscellaneous regulated products: two novel foods, one flavouring and one food additive
This consultation seeks stakeholders’ views, comments and feedback in relation to the regulated product applications considered in this document, which have been submitted for authorisation.
Summary of responses
This consultation will be of most interest to:
- Food industry trade associations.
- Food business operators in the UK wishing to use the novel foods, flavouring or food additive.
- Enforcement Authorities, including Local Authorities, Port Health Authorities and District Councils.
- Consumers and wider stakeholders.
A list of interested parties is included in Annex A.
Consultation subject and purpose
This consultation seeks stakeholders’ views, comments and feedback in relation to the regulated product applications considered in this document, which have been submitted for authorisation (either as new authorisations or for extension of use / modification). We ask stakeholders to consider any relevant provisions of retained EU law and other legitimate factors (other evidence further supporting clear, rational and justifiable risk analysis, such as consumer interests, technical feasibility and environmental factors), including those that the Food Standards Agency (FSA) and Food Standards Scotland (FSS) have identified as relevant to these applications. This is stakeholders’ opportunity for input on the advice given to Ministers to inform decision making.
The consultation concerns the following regulated products:
- RP1158 Vitamin D2 mushroom powder - novel food
- RP1292 UV-treated baker's yeast (Saccharomyces cerevisiae) – novel food
- RP1382 3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)-1-(3-hydroxybenzyl)imidazolidine-2,4-dione – flavouring
- RP1194 Rebaudioside M – food additive
The FSA/FSS scientific opinions, and the views gathered through this consultation, will be considered and included alongside those of officials across the FSA, FSS and, for novel foods, UK Government Departments other than the FSA to inform Ministers’ decision-making on whether to authorise the individual regulated products for use in Great Britain (GB).
A parallel consultation is being published by FSS.
Read the full consultation pack
Consultation on applications for authorisation of miscellaneous regulated products: two novel foods, one flavouring and one food additive (accessible version)
How to respond
Response to this consultation should be submitted via the online survey (Microsoft forms). If this is not possible you can email a response to:
Email: RPconsultations@food.gov.uk
Name: Regulated Products Approvals Team
Division/Branch: Regulated Services
Publication of response summary
Within three months of a consultation ending we aim to publish a summary of responses received and provide a link to it from this page.
You can find information on how we handle data provided in response to consultations in our Consultations privacy notice.
Further information
This consultation has been prepared in accordance with HM Government Consultation Principles. If an Impact Assessment has been produced, this is included in the consultation documents. If no Impact Assessment has been provided, the reason will be given in the consultation document.