Professional documentation and compliance

Solutions

End-to-end support for your functional ingredient needs, from selection to delivery

Solutions Overview

Comprehensive support across the ingredient lifecycle

Ingredient Selection & Substitution

Matching based on application targets, cost range, and target market.

Document Package & Compliance Preparation

Collaboration on Spec/COA/SDS/Declaration documents.

Application Support

Samples, application advice, formulation directions, and evaluation points.

Supply Chain Delivery Collaboration

Lead time, batch, shipping, and customs clearance document collaboration.

Quality Communication Mechanism

Batch consistency, deviation communication, and traceability support.

Typical Cooperation Process

A streamlined approach from initial inquiry to ongoing optimization

1

Confirm Application Scenario and Target Market

Understanding your product requirements, target applications, and regulatory environment.

2

Provide Ingredient Recommendation List and Document Pre-review

Availability assessment, key compliance points evaluation for your target market.

3

Sample and Application Verification

Testing inclusion level, flavor characteristics, and stability points in your formulation.

4

Quotation, Supply, and Delivery Plan

Detailed planning for batch/lead time/shipping to ensure seamless supply.

5

Quality Communication and Continuous Optimization

Ongoing support for re-ordering and solution iteration based on your feedback.

Quality & Compliance

Traceable

Batches and documents are traceable

Verifiable

Key information is verifiable via formal documents

Document Supportable

Comprehensive packages per market demand

Document Package List

Available upon request

Specification

COA (Certificate of Analysis)

SDS (Safety Data Sheet)

Declaration Documents

Allergens / GMO / Irradiation / Heavy Metals, etc.

Compliance Status Summary

Based on target market and document availability

Disclaimer: The regulatory and compliance information provided on this website is for general reference only and does not constitute legal advice or regulatory commitments; specific matters are subject to the requirements of the target market's competent authorities and the supplier's formal documents.

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