// CUSTOM FORMULATION
Turn ingredient, serving and format requirements into a supplier development brief. Nutrivelta coordinates feasibility questions, sample scope and the responsibilities needed for a custom-formulation proposal.
A custom brief begins with the intended composition and market requirements. The responsible supplier and technical reviewers assess the formula, process and samples; the written scope records ownership, approvals and commercial conditions.
// 01 / BRIEF
Set out the intended ingredients, amounts per serving, format and audience. Include restrictions and the market requirements the proposal needs to address.
// 02 / FEASIBILITY
Identify the supplier and technical review responsibilities. Compare proposed formula changes, process constraints and sample evaluation criteria before selecting the development route.
// 03 / AGREEMENT
Record confidentiality, formula ownership, development deliverables and approval roles. Carry the selected formula and artwork versions into the written quotation and order.
// HOW TO GET STARTED
Describe ingredients, intended amounts, serving, format, market and restrictions.
Identify technical questions, proposed changes and the party responsible for evaluating them.
Record deliverables, confidentiality, formula-use rights, costs and review responsibilities.
Use agreed criteria for composition, presentation, sensory characteristics and any required testing.
Resolve the review findings and identify the specification, package and label for the proposal.
Record the quantity, schedule, documents and responsibilities for the proposed order.
// YOUR PROJECT INPUTS
Use these points to prepare the first discussion. Include what you know and identify the decisions you still need to make.
// BEFORE THE BRIEF
Share the ingredients, intended amounts per serving, preferred format, target market and expected quantity. We coordinate the supplier feasibility discussion and identify the proposed development work, samples and responsibilities.
The supplier quotation sets the minimum for the selected formula, format, packaging and unit of measure. Label-only changes, a different pack and a new formulation can have different order conditions; include the intended configuration in your brief.
Tell us which product or formula you want to evaluate and the questions the sample should answer. Sample type, version, quantity, charges, shipping and evaluation scope are agreed before an arrangement is made.
Formula review, sample evaluation, packaging, artwork approval, production, release and dispatch have separate dependencies. The written proposal sets the milestones for the agreed product, quantity and responsible parties.
// FOR YOUR PRODUCT BRIEF
| What to compare | Why it matters | What to request |
|---|---|---|
| Technical starting point | An ingredient wish list is not the same as a workable formulation proposal. | The requirements, constraints and questions for the responsible supplier to evaluate. |
| Sample and approval scope | A sample should be evaluated against an agreed version and criteria. | The proposed sample version, acceptance questions and sign-off responsibilities. |
| Ownership and handover | Development, manufacturing and formula rights are different responsibilities. | Written confidentiality, ownership, change-control and delivery terms relevant to the project. |
The review considers the actual ingredients, amount basis, format, process requirements, restrictions and intended product. Its output should identify proposed changes, open questions, samples and the development work needed for a quotation.
The project identifies the supplier and technical parties performing the work, their deliverables and approval roles. Nutrivelta coordinates that brief and handover; the proposal should name the parties responsible for formulation, manufacturing and review.
// YOUR NEXT STEP
Share your ingredients, intended amounts per serving, format and market. Include restrictions, pack requirements and the work you want the supplier to assess.
