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Supplier Compliance

Supplier Compliance Documents Checklist for Major Buyers

Zilch Team · · Checklist

Major buyers can ask for evidence about your business, the suppliers behind it and the products you sell. Getting that information together before the next tender is much easier than doing it with an order on hold.

This checklist covers 15 common evidence categories for wholesalers and distributors. It is a starting point for building your records, not a statement that every item is legally required for every business or product.

Use the actual buyer specification and applicable rules to decide what is needed. For each relevant item, record the owner, scope, current version and next action. For an item that does not apply, keep the reason.

1. Business identity and contracting details

Keep your legal entity name, ABN or other relevant registration, trading names, business addresses and authorised contacts consistent.

The entity supplying the goods should agree with the entity in the contract and supporting company documents. Explain group structures where a policy or certificate belongs to a parent or related business.

These details are easy to overlook because they feel basic. A mismatch can still stop onboarding while the buyer asks which entity it is actually approving.

2. Insurance certificates of currency

Keep the insurance evidence the buyer requests, which may include public liability, product liability or other cover relevant to the activity.

Check the insured entity, policy period, cover type and required limits. A certificate of currency is evidence of a policy; it does not replace reviewing the relevant policy terms or confirming that the activities are covered.

Give responsibility for renewals to a named person and record which customer requirements depend on the document.

3. Supplier code of conduct and acceptance records

Buyers may ask you to accept their code, provide your own supplier code or explain how expectations are communicated upstream.

Keep the approved version and evidence of relevant acceptance or implementation. A downloaded template sitting in a folder does not demonstrate that suppliers have agreed to it.

The Commonwealth Supplier Code of Conduct is one example of an explicit procurement framework. Assess the code that applies to the actual contract rather than substituting a generic policy.

4. Modern slavery and human rights evidence

Depending on the request, keep the relevant policy or statement, supply-chain risk assessment, due-diligence records and evidence of action taken.

The buyer may need information even where your business does not have its own statutory statement obligation. Its questionnaire and your legal reporting position are separate questions.

Government modern slavery procurement resources show the kinds of supplier information that can be requested. Answer according to your actual practices and identify gaps honestly.

5. Supplier and manufacturing site information

Record which suppliers and factories are connected to the products you sell. Keep addresses, entity names and the basis for country-of-origin information where relevant.

Distinguish the manufacturer's location from the location of a wholesaler or sales office. Also distinguish country of manufacture from the origin of every material or component.

Set access rules for commercially sensitive factory details. If a buyer needs disclosure for due diligence, agree a suitable method rather than sending an unqualified assurance with no supporting information.

6. Ethical audit reports and corrective actions

Where requested, retain reports such as SMETA or other relevant factory audit evidence, with the audited site, date, scope and follow-up information.

Read the findings and corrective actions. A report's existence does not mean the site has no issues or that every concern has been resolved.

Sedex explains that SMETA and Sedex membership are not certifications. Avoid turning an audit into a product badge that implies a broader approval than the evidence supports.

7. Management system certificates

Keep relevant certificates for systems such as quality, environmental or occupational health and safety management when the buyer requires them.

Confirm the certified organisation, sites, standard, scope and current status. A certificate held by a manufacturer does not automatically certify the distributor selling its products.

Where the requirement concerns your own business, be explicit about whether you hold the certification or rely on a supplier's certified system. Those answers are commercially different.

8. Product specifications and material information

Retain the specification that identifies the product, model, materials, dimensions and other attributes relevant to its intended use and buyer requirements.

For products with variants, make clear which attributes differ. A change to a coating, battery, fabric or component can affect the relevance of other supporting evidence.

Keep estimated or modelled material information distinguishable from manufacturer-confirmed specifications. A useful estimate for sustainability assessment should not quietly become an authoritative engineering specification.

9. Product test reports

Keep reports supporting the tests required for the product and market. Check the model, sample identity, standard and version, laboratory and test scope.

A report for a similar-looking product may not cover yours. Nor does a report remain applicable regardless of later changes to materials or construction.

Set review triggers based on the product, applicable requirement and buyer expectations. Avoid inventing a universal expiry date for every test report.

10. Declarations of conformity and regulated product records

Some products and regulatory schemes require formal declarations, registrations or other compliance records. Identify the applicable scheme and responsible entity before preparing the paperwork.

For example, ACMA's supplier guidance sets out steps for products within its scope, including compliance evidence and declarations.

A generic statement generated from a product description does not establish conformity. The person signing should understand the evidence and the particular requirement being declared.

11. Safety data sheets

For relevant chemical products, retain the appropriate current SDS and connect it to the exact product supplied.

Check the revision information and Australian supplier or importer details where required. Establish how customers receive the correct document and how updates are managed.

Not every catalogue item needs an SDS. Safe Work Australia's guidance explains scope and exemptions. For operations in Victoria, also use WorkSafe Victoria's guidance.

12. Restricted substance and PFAS evidence

Keep supplier declarations or test evidence addressing the specific restrictions and buyer policies relevant to your products.

Record the substances, threshold, product scope and information source. A statement about PFOA alone should not be presented as an all-PFAS declaration.

For laboratory evidence, preserve sample identity, tested substances, method and reporting limits. The word "passed" without those details may tell you very little about whether the customer's requirement was assessed.

13. Certification and chain of custody evidence

For certified material or sourcing claims, keep the relevant certificate and any product or transaction evidence required by the scheme.

Check which organisation and products are covered, whether the claim is permitted and what documentation is needed through the supply chain. Do not assume a supplier's certificate applies to every item in its catalogue.

Textile Exchange's scope and transaction certificate policy illustrates why different records serve different purposes. Follow the specific scheme behind your claim.

14. Sustainability and environmental claim evidence

Retain the evidence supporting claims about recycled content, emissions, recyclability, compostability or other environmental attributes.

For carbon figures, identify the product unit, calculation boundary, methodology and whether the result is modelled, supplier-provided or independently verified. Keep limitations that affect comparison visible.

The ACCC's environmental claims guide is a useful reference for reviewing public statements. A claim on a quote or product page needs the same care as one on a large advertising campaign.

15. Approved answers and the final customer submission

Keep the questionnaire or tender response actually sent, the supporting attachments, approvals and buyer clarifications.

Retain reusable answers separately from commitments specific to that customer. Record when changing evidence should trigger a review of an existing answer.

This final record closes the loop. Without it, you may know what documents exist but be unable to establish what was represented to the buyer at the time.

Turn the checklist into a useful register

For each applicable requirement, record the company, supplier, site or product it concerns; the evidence held; the reviewer; and the next action. Add the source requirement so staff know why the item is needed.

A checklist summary like the example below should include the evidence category, applicability, owner, current status and review trigger. Keep the detailed documents linked rather than copying every explanation into the summary.

Example register entries
Evidence categoryApplies?OwnerStatusReview trigger
Insurance certificates of currencyYes. The buyer requires public and product liability coverFinance managerAcceptedPolicy renewal
Ethical audit reportsYes, for three factoriesSourcing managerTwo accepted, one awaiting corrective action follow-upNew audit or corrective action closed
Product test reportsYes, for the tendered rangeProduct managerReceived, under reviewChange to materials, construction or the applicable standard
Safety data sheetsNo. The range contains no hazardous chemicalsCompliance leadNot applicable, basis recordedChemical products added to the range
Restricted substance and PFAS evidenceYes. The buyer's policy requires no intentionally added PFASCompliance leadSupplier declarations requestedSupplier, treatment or buyer policy change
Illustrative entries for a distributor preparing a tender response.

Do not use a simple file count as your compliance measure. Forty PDFs may cover five products well and leave the rest of the catalogue unresolved.

Separate received evidence from accepted evidence. A report can be present and still require clarification because the relevant model is missing or the issuing entity cannot be verified.

Prioritise the gaps that affect current business

Start with legal requirements and product-safety concerns, then the evidence needed for active customer approvals and significant upcoming opportunities.

Assign the next action rather than just marking the cell red. A missing SDS needs a request to the responsible source. An unclear test scope needs technical review. An unsigned policy needs an internal decision and implementation.

Where a requirement does not apply, retain the basis. That avoids collecting unnecessary paperwork every time a new employee reviews the account.

Keep the records connected to sales

The evidence should be available when an account manager needs to answer a buyer, without giving every salesperson unrestricted access to sensitive source files.

Use approved responses and appropriate customer-facing reports. Preserve complete originals and required safety information. The person sharing a document should know whether it is relevant and permitted to leave the business.

Zilch helps distributors organise this evidence across company, supplier and product records and reuse it in buyer responses. Bring an active customer request to a walkthrough to see which requirements you can already answer and which gaps still need attention.

Sources and further reading