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HomeGlossaryUK FIR (Regulation 1169/2011 retained) — supplement labelling
Compliance

UK FIR (Regulation 1169/2011 retained) — supplement labelling

In short

The UK Food Information Regulations 2014 (SI 2014/1855) and the retained EU Regulation 1169/2011 (FIC) set the mandatory food-information rules that apply to food supplements as well as foods: the name of the food, ingredient list with allergens emphasised, net quantity, durab...

The UK Food Information Regulations 2014 (SI 2014/1855) and the retained EU Regulation 1169/2011 (FIC) set the mandatory food-information rules that apply to food supplements as well as foods: the name of the food, ingredient list with allergens emphasised, net quantity, durability date, business name & address, country of origin where required, and minimum 1.2 mm x-height type. Plus the supplement-specific composition box from the 2003 Regulations.

Regulatory anchors
  • SI 2014/1855
  • Regulation (EU) 1169/2011 (retained)
How V5 handles it
QMS — quality records next to the work they concern.
Deviations, corrective actions and quality review sit in the same system as production, so each quality record references the work order, step and lot it concerns.
Document control — one version in force, every change signed and explained.
Draft the next revision while the current one stays in use, approve it under your sign-off route, and track training on it — with the history kept.
Score your compliance gap — then download the validation pack.
A guided self-assessment walks you against the regulator clauses that apply to your industry. The validation pack — IQ/OQ scripts, traceability matrix, risk assessment, intended-use statement — generates from the same evidence so you can hand it to an auditor on day one.
Related terms
UK Food Supplements (England) Regulations 2003UK CAP Code & ASA enforcement (supplement claims)
Software that covers UK FIR (Regulation 1169/2011 retained) — supplement labelling
V5 Ultimate Dietary Supplements
Written for supplement contract manufacturers and brand owners tired of surviving FDA 483s on paper.
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