Sourcing Resources & Downloads

A public checklist and documents to request for review

Editable sourcing & project tools

Public planning template, not a COA, TDS, certificate, approved specification or manufacturing commitment. Fill only nonconfidential requirements; unknowns may be “to discuss”. Keep confidential formulas out of public forms. Documents, supply, executors, costs and schedule require written confirmation.

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Ingredient sourcing brief & supplier document review

Version: 2026-09-08

Download editable template (Markdown) Bilingual sourcing checklist (TXT)

Buyer requirements

  • Company / contact / email; project reference and date________________
  • Ingredient / botanical identity / plant part; proposed SKU if known________________
  • Target marker, method and limits requested; solvent / carrier / origin requirements________________
  • Application, target countries, intended use level; pH / heat process / packaging________________
  • Sample quantity and acceptance criteria; first order / annual estimate with units________________
  • Destination, desired date, budget currency; packaging / Incoterms to discuss________________

Supplier document review — record evidence, not assumptions

  • For each requested file record: document name / SKU or lot / version-date / issuer / received date / reviewer / gap / next action________________
  • TDS: match identity, composition, methods, limits, storage and shelf-life basis to offered SKU________________
  • Genuine lot COA: match lot and specification; review actual results, units, methods and applicable contaminant limits. A sample COA does not release a future lot________________
  • Certification if required: holder, legal entity, site, scope, issuer, number, validity and verification source. A logo is not evidence________________
  • Traceability / allergen / residual-solvent / import documents: list applicable requests and missing items________________
  • Disposition: pending evidence / clarify / acceptable for stated review scope / not acceptable; reviewer and date. Do not equate document review with shipment release________________

Written next-step agreement

  • Confirm source (own / partner / custom), availability, sample fees/freight, MOQ, lead time, quote validity, payment and responsible contact before ordering________________

Concept-stage ODM project brief

Version: 2026-09-08

Download editable template (Markdown)

Nonconfidential starting point

  • Company / contact / email; project reference and date________________
  • Target audience, occasion and target countries; intended product category________________
  • Beverage format, flavor and sweetness preferences; reference concept (not a validated formula)________________
  • Candidate ingredients / exclusions / allergens; claims needing local review (not approved claims)________________
  • Packaging direction, desired shelf life and storage conditions to validate________________
  • Budget currency / range, initial quantity with units and desired timing; unknowns to discuss________________

Proposed stage gates — agree before execution

  • Brief review: customer approves scope, unknowns and candidate-material document requests________________
  • Prototype: name R&D executor; agree fees, iterations, sensory criteria and safety/market review before work________________
  • Validation: name testing executor; agree protocol, packaging, stability criteria, records and stop/go decision owner________________
  • Production feasibility: confirm qualified partner/site/line, pilot criteria, IP, release responsibility, costs and delivery scope in writing________________
  • Next action / owner / due date / evidence needed; no project is accepted by completing this template________________

Existing-formula transfer review checklist

Version: 2026-09-08

Download editable template (Markdown)

Public first-contact summary

  • Company / contact / email; project reference and date________________
  • Nonconfidential format, target countries, packaging, process stage and completed trials________________
  • Formula ownership or authorization status; NDA contact and approved secure handover method to agree before sharing________________
  • Initial volume with units, schedule and budget currency; known transfer constraints________________

Controlled technical handover — inventory only, no formula here

  • Record owner / version / availability / gap for formula and BOM, raw-material specifications, process flow and critical parameters________________
  • Inventory trial reports, analytical methods, packaging specifications and stability evidence; agree secure access after confidentiality approval________________
  • Compare proposed executor/site/line capability with process and packaging needs; document gaps rather than assume compatibility________________
  • Agree pilot plan, change control, deviations, acceptance/rejection criteria and stop/go owner________________
  • Assign market/label review, testing, batch release, traceability, IP and retained-record responsibilities________________
  • Written feasibility outcome: pending evidence / pilot review / not feasible; named executor, quote, MOQ and schedule remain to confirm________________

The documents below must be requested by product and intended use, subject to availability and applicable scope. No downloadable certificates or product catalogue are published here.

Certificate of Analysis (COA)

Specify product, grade and batch if known. Request the relevant batch tests, limits, results and methods; an example is not evidence for a future shipment.

Request review: Certificate of Analysis (COA)

Technical Data Sheet (TDS)

Specify assay, method, carrier, solubility and use case to request the technical information for the relevant grade.

Request review: Technical Data Sheet (TDS)

Certification copy review

State the required standard and market. Review the entity, site, product scope and validity. This listing does not claim that any product is certified.

Request review: Certification copy review