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A clearer route to your next ingredient

Botanical ingredient buyer resources

Move from a product name to an evidence-backed purchasing brief. Start with the specification, collect the right documents, and make unresolved questions visible.

Your sourcing workflow

  1. 01

    Define the article

    Choose the species, plant part, grade, assay basis, and formulation requirements.

    Read the buying guides →
  2. 02

    Review the evidence

    Separate growing origin, manufacturing site, process, and lot-level documents.

    Explore the ingredient pages →
  3. 03

    Compare the offer

    Normalize comparable prices and include the acquisition costs in your own quote.

    Use the free tools →
  4. 04

    Prepare a request

    Put unresolved questions and commercial requirements in a written brief.

    Build your RFQ →

Supplier document checklist

Use this to organize your document request. Your technical and quality teams set the acceptance criteria and determine what evidence is sufficient for your intended product.

0 of 8 document groups collected. This tracks your checklist, not supplier approval. Selections reset when you leave.

Compare these documents across suppliers in the evidence scorecard →

Open research

See our evidence coverage

Inspect the directory’s research footprint and download the underlying counts. Clear denominators, dates, and limitations.

Further reading

Explore the article archive

Background reading on sourcing, testing, pricing, and documentation. Articles are separate from supplier scores.

Primary-source references

FDA’s guidance explains that dietary-ingredient identity testing and reliance on supplier COAs are distinct requirements. A COA alone does not replace the applicable identity-testing requirement. Where reliance on a supplier COA is permitted, supplier qualification and appropriate documentation are required. Read FDA’s dietary supplement CGMP guide.

A food facility registration number is not FDA approval or endorsement of a facility or its products. Read FDA’s food facility registration Q&A. References checked November 15, 2026; your qualified team should determine the requirements applicable to your operation.

From research to a sourcing brief

Tell us what you need to source.

Describe the grade, quantity, destination, and evidence you need. Inquiries are free and reviewed by CleanIngredients. Availability and supplier acceptance are not guaranteed.