Which document you need and why
CU TR 005/2011 declaration for packaging within scope
The declaration confirms applicable safety requirements for finished packaging and closures by material and use. Medical, pharmaceutical, tobacco and dangerous-goods packaging must be checked against exclusions; packaging made during production by the packaged-product manufacturer follows special provisions. Food contact alone does not automatically mean a separate state registration certificate: CU TR 005 and sanitary-list applicability must first be distinguished.
What to send for a quotation
Start with these four items. If something is missing, send what you have and we will explain what else is needed.
Product name
Name, model, intended use and manufacturer.
HS / EAEU commodity code
Include the code if known. If not, we can help identify the product.
Technical description
Specifications, photographs, instructions or a product datasheet.
Composition and materials
Ingredients, materials or a component specification, depending on the product.
Specify container size and shape, layer structure, colourants, printing and closure method. Include contents’ fat/acidity, temperature and contact duration, hot-fill or reuse conditions, and the sizes and materials proposed for one declaration.
Which requirements we check
- Material and use by group
- Food-contact conditions and simulants
- Strength and leak tightness
- Relevant substance migration
- Material identification and symbols
- Justification for grouping sizes, layers and manufacturers
How the process works
- 01
Product
Review the description and identify the required document.
- 02
Assessment
Check the records and arrange any required testing.
- 03
Documentation
Support the documentation and registration procedure.
- 04
Your document pack
Deliver the completed documents and agreed work results.
What you receive
- Registered declaration after completing the applicable procedure
- Included packaging test reports
- Evidence and product descriptions
- Checked marking information and intended-use limits
Sources & regulatory basis
Timing & cost
Quoted after reviewing models, manufacturers, testing scope, site visits and translation needs. The proposal separates the stages and their deliverables.