CHINA PURCHASE ORDER CHECKLIST

China Purchase Order Checklist for Importers

A practical checklist for importers preparing and reviewing a purchase order before a Chinese supplier begins production.

By Kelsy Founder, Kelsy Sourcing Published: Jul 13, 2026
Purchase order, product specification sheets, approved sample references, packaging instructions, pricing details, and supplier confirmation records prepared for importer review.

Turn approved requirements into one controlled production order

Connect the supplier, product, price, specification, sample, packaging, payment, inspection, and delivery terms before production begins.

Clear order baseline
Production-ready details
Owned milestones
Controlled changes

A purchase order should tell the supplier exactly what the buyer has approved, what must happen next, and what evidence is needed before payment or shipment. If a supplier still has to search through chat messages to understand the order, the PO is not ready for production.

This checklist is for importers placing production orders with Chinese suppliers. Work through it after the quotation, product specification, sample, packaging plan, and commercial terms have been reviewed, but before anyone authorizes materials, tooling, printing, or mass production.

Treat the PO as the control page for a larger order file. It should point to the correct specifications, artwork, sample records, inspection criteria, and shipping instructions instead of trying to compress every technical detail into one document. Every referenced attachment needs a clear name, date, and revision.

The legal effect of a PO, and whether it takes priority over a quotation, pro forma invoice, contract, or supplier terms, depends on the documents, the governing law, and the parties’ conduct. For large orders, custom development, intellectual property, breach remedies, or dispute provisions, obtain advice from qualified legal counsel. A PO does not replace a suitable contract, technical specification, or inspection plan.

If supplier identity or authority is still uncertain, complete the China Supplier Verification Checklist before issuing the order.

1. Confirm the Buyer and Supplier Legal Entities

Enter the buyer’s full legal name, registered address, billing details, tax or registration information where relevant, and the contact authorized to issue the PO. Do the same for the supplier that will accept the order. A trading name, marketplace profile, or salesperson’s nickname is not enough to identify the contracting party.

Compare the supplier name with its business records, quotation, pro forma invoice, bank beneficiary, and any signed agreement. Differences may have a legitimate explanation, such as an export company receiving funds for a factory, but the relationship and responsibility should be documented before the PO is released.

List operational contacts separately from the legal entities: sales, engineering, quality, finance, and logistics. This prevents a production question from being treated as a contract change simply because it was discussed with the wrong person. Record who may approve specifications, prices, changes, and shipment release on the buyer’s side.

2. Assign a Unique Purchase Order Number

Give the PO one unique number that appears on the pro forma invoice, payment request, packing list, inspection booking, shipping documents, and internal records. The number should not be reused for a repeat order unless the buyer’s control system clearly distinguishes each release.

A useful PO header also shows issue date, buyer project number, supplier quotation reference, currency, and current revision. These details let finance, quality, and logistics confirm that they are looking at the same order without relying on a file name such as final-new-2.pdf.

Keep a simple register showing the PO number, supplier, order value, owner, status, latest revision, and key dates. This becomes the starting point when a colleague needs to find an approval, explain a variance, or reconcile documents months later.

Purchase order control header
FieldWhat to enterWhy it matters
PO numberOne unique buyer-controlled referenceConnects every order record
Issue and revisionIssue date, revision code, and revision dateShows which version is current
Source quotationSupplier quotation or PI number and datePreserves the commercial basis
Buyer ownerName and approval authorityClarifies who can release or change the order
Use the same control references across commercial, quality, and shipping records.

3. Reference the Approved Quotation

Identify the exact supplier quotation used to prepare the PO, including its number, date, revision, and validity period. If negotiation happened in several email threads, ask for a clean revised quotation or prepare a comparison record that explains which prices and conditions were accepted.

Before copying figures into the PO, use the supplier quotation comparison guide to normalize specifications, included costs, MOQ, lead time, payment terms, and exclusions.

The PO should resolve conflicts rather than carry them forward. If the quotation says neutral packing but the approved order requires printed retail boxes, state the final requirement and adjusted price. If a quotation item was rejected, remove it or mark it clearly as not ordered.

4. Identify Every Product and Variant

Create one line for each product, model, size, color, material, voltage, plug, language, pack configuration, or other variant that changes what the supplier must make. Use the buyer’s SKU and the supplier’s model code when both exist, so warehouse and factory records can be reconciled.

Avoid generic descriptions such as blue bottle or standard adapter. The line should be specific enough that a person who did not join the negotiation can match it to the correct drawing, sample, artwork, and packaging instruction. Photographs can help identify an item, but they should not replace measurable requirements.

Check that variant totals agree with the overall quantity and carton plan. When mixed colors or assortments are permitted, state the quantity per variant and whether substitutions need written approval. Do not leave a range for the factory to allocate later.

Purchase order line-item record
Buyer SKUSupplier codeProduct and variantQuantity and unitSpecification reference
KS-101-BLKFactory model A17Black, 500 ml, EU label2,000 piecesSPEC-101 Rev C
KS-101-WHTFactory model A17White, 500 ml, EU label1,000 piecesSPEC-101 Rev C
Use a separate row when any production or packing requirement differs.

5. Attach the Final Product Specification

Reference the approved specification by document title, number, revision, and date. It should cover the attributes that determine acceptance: materials, dimensions and tolerances, components, performance, finish, color standard, workmanship, safety features, regulatory markings, and test methods relevant to the product.

If requirements are still scattered across chats and supplier files, organize them with the Order Requirements Checklist before releasing the PO.

Resolve phrases such as high quality, export standard, same as before, or suitable packaging. They are not measurable. Where a tolerance or test is still open, name the owner, decision date, and production hold point. An unresolved critical requirement should remain a release blocker, not a note for later.

6. Link the PO to the Approved Sample

If the order depends on a sample, record the sample approval ID, approval date, photographs, courier tracking, location of the retained sample, and any approved deviations. State whether the sample is a visual reference, functional reference, packaging reference, or full golden sample.

Use the Sample Approval Checklist to document what was checked, what remains different, and which version the factory must follow.

Do not write same as sample without identifying the sample. Suppliers may have several prototypes, and the buyer may have approved only part of one version. If mass production must improve a sample defect, describe the correction in the specification and PO rather than expecting the factory to infer it.

7. Confirm Quantity and Unit of Measure

State the ordered quantity for every line and the unit of measure: pieces, sets, pairs, kilograms, meters, cartons, or another defined unit. Confirm how many individual units make one set and whether accessories are included in that count.

Record the allowed quantity variance only if the buyer accepts one. If overproduction, underproduction, process loss, or print overruns require approval, say so. Also state how invoicing will be handled when the shipped quantity differs from the PO quantity.

Check the arithmetic at three levels: line quantity, variant subtotal, and order total. Then compare it with MOQ, inner-pack count, master-carton count, container plan, and expected spare quantity. Small inconsistencies here often become production or freight problems later.

8. Verify Unit Price, Currency, and Order Total

Show the unit price, price basis, currency, line total, adjustments, and grand total. Specify the number of decimal places used and make sure multiplication and rounding produce the same total on the PO and supplier PI.

Separate product charges from tooling, samples, testing, packaging, printing, domestic freight, export documents, or other one-time fees. If a fee was prepaid or will be credited, show the credit and remaining amount rather than relying on finance to remember an earlier transfer.

For a deeper commercial review, follow the Pricing, MOQ & Quotation Guide and reconcile the final PO against the approved cost sheet.

9. State What the Price Includes and Excludes

A unit price is incomplete until its inclusions are defined. State whether it covers standard or custom packaging, labels, accessories, spare parts, testing, inspection support, loading, export clearance, local transport, bank fees, taxes, and delivery to the named Incoterm place.

List known exclusions that the buyer will arrange or pay separately. This is especially important when the supplier quote looks low because molds, printing plates, compliance testing, certificates, pallets, or inland freight are omitted.

Where the final cost depends on an estimate, such as raw-material surcharge or freight, state the adjustment rule, evidence required, approval owner, and deadline. The supplier should not treat an open estimate as permission to increase the PO total without a written revision.

10. Define Packaging Requirements

Specify unit packaging, inner pack, master carton, protective materials, sealing method, palletization, carton dimensions, gross and net weight limits, and any drop, compression, moisture, or transit requirements. Link to drawings or packaging specifications by revision.

Review the complete packaging handoff with the Private Label & Packaging Checklist before printed materials or cartons are ordered.

Confirm packing quantity and orientation for every SKU. If mixed cartons are allowed, define the assortment and carton mark. If packaging must pass a test or buyer approval, place that event before mass printing or production release and identify who signs it off.

11. Control Branding, Labels, and Artwork

List every logo, label, barcode, warning, instruction, insert, carton mark, country-of-origin mark, and regulatory symbol required for the order. Reference controlled artwork files by name, revision, dimensions, color standard, material, finish, and placement.

State whether the supplier must provide a digital proof, printed proof, pre-production sample, barcode scan, or first-off photograph before continuing. Define the approval channel and make clear that approval applies only to the identified revision.

Check product, market, and customer requirements before printing. The supplier can follow artwork supplied by the buyer, but that does not automatically establish that claims, translations, barcodes, trademarks, or regulatory labels are correct for the destination market.

12. List Accessories, Components, and Spare Parts

For each sellable unit, list the exact accessories and components that must be packed with it: cables, adapters, fasteners, batteries, manuals, tools, pouches, replacement parts, or promotional inserts. Include quantity, specification, color, and pack location.

If the buyer orders spare units or spare components, place them on separate lines and explain whether they are free, included in the unit price, or separately charged. State whether spares ship in bulk, inside cartons, or as individually labeled service parts.

Confirm compatibility where components come from different sources. A cable may fit physically but fail the required current rating; a cap may match the thread but use a different material. Reference the component specification and inspection method instead of relying on its familiar name.

13. Record Tooling and Mold Terms

Identify every mold, die, jig, fixture, printing plate, cutting tool, or custom development item associated with the order. Record price, payment stage, ownership, storage location, expected life, maintenance responsibility, and the product or drawing it supports.

State whether tooling is new, modified, shared, or transferred from another supplier. For buyer-owned tooling, address identification marks, access, permitted use, sample retention, maintenance records, and the process for return or transfer.

Tooling ownership and intellectual-property rights can require contractual language beyond a PO. For material investments or custom designs, ask qualified counsel to review ownership, confidentiality, permitted use, breach, and dispute provisions before payment or production.

14. Define When Lead Time Starts

Do not record lead time only as 30 days. Define the event that starts the clock: receipt of deposit, signed PO, approved artwork, approved sample, confirmed material, or completion of all release conditions. If several conditions apply, say that lead time starts after the last one is completed.

Ask the supplier to confirm material procurement time, production time, packing time, inspection readiness, rework allowance, and handover time. This exposes whether the quoted lead time covers the full order or only factory processing.

Record any buyer-dependent dates, such as artwork approval or component delivery. When a buyer action is late, update the schedule through a controlled revision rather than leaving both parties with different assumptions about the original delivery date.

15. Set Delivery Dates and Milestones

Convert the lead time into calendar dates for critical events: order release, material confirmation, first production, in-process review, packing completion, inspection readiness, corrective action, final handover, and required arrival where known.

After release, track these events with the China Production Follow-Up Checklist instead of asking only whether the order is on schedule.

For each milestone, name the supplier owner, buyer reviewer, evidence required, and consequence of delay. A status message should be supported by appropriate records such as material photographs, production counts, test results, packing data, or inspection readiness confirmation.

Production and delivery milestones
MilestoneTarget dateRequired evidenceOwner or approver
Production releaseAgreed calendar dateSigned PO and closed release checklistBuyer order owner
Materials readyAgreed calendar dateMaterial records or first-off evidenceSupplier production lead
Inspection readyAgreed calendar dateQuantity, packing status, and inspection bookingSupplier quality lead
Goods handoverAgreed calendar dateRelease approval and shipping documentsSupplier logistics lead
Replace relative lead-time promises with dated control points.

16. Confirm the Incoterm and Named Place

State the selected Incoterm rule and version, together with a precise named place, port, terminal, or destination. FOB China or EXW factory is too vague when several ports, facilities, or handover points are possible.

Confirm which party arranges export clearance, inland transport, loading, main freight, insurance, import clearance, duties, and final delivery. The commercial handover point should match the price, shipping plan, and documents the supplier is expected to provide.

An Incoterm allocates certain costs, tasks, and risks, but it does not by itself define product quality, payment timing, title, remedies, or every shipping service. Record those matters in the appropriate PO, contract, specification, and logistics instructions.

17. Write Payment Terms as Amounts and Conditions

State the payment currency, percentage or fixed amount, due date or trigger, beneficiary requirements, and bank-fee treatment for each stage. Check that deposit and balance calculations add up to the approved total after credits and prior payments.

Before sending any supplier funds, follow the China Supplier Payment Checklist to verify the PI, bank instructions, approvals, milestone, and transfer record.

Do not let the PO normalize unexplained third-party accounts or last-minute bank changes. If the beneficiary differs from the supplier, document the business relationship, obtain appropriate invoices or agreements, verify through known contacts, and check with finance, the bank, or professional advisers as the risk requires.

18. Connect Payment to Production and Inspection Milestones

A payment stage should be tied to evidence rather than a calendar date alone. For example, a deposit may follow an accepted PO and verified PI; a progress payment may require an approved first article; and a balance may require completed production, passed inspection, closed corrective actions, and agreed shipping documents.

Define what passed means, who can approve it, and how exceptions are handled. If an inspection finds defects, the order file should show whether the supplier reworks, replaces, discounts, or receives a conditional release and who accepted that decision.

Payment control does not guarantee performance, and withholding money without a contractual basis can create its own dispute. Align milestone conditions with the signed commercial documents and obtain legal advice when rights, remedies, or a serious breach are contested.

19. Specify Inspection and Quality Requirements

State which inspections or tests apply: incoming material, first article, in-process, pre-shipment, loading supervision, laboratory testing, or document review. Identify the standard, sample size or method, defect classification, acceptance criteria, and required reports.

Build the final inspection brief with the China Pre-Shipment Inspection Checklist and book the activity early enough to allow review and corrective action.

Clarify who appoints and pays the inspector, where inspection occurs, how much production must be complete, and whether goods must be packed. Require the supplier to provide access, samples, equipment, and records. Inspection reduces uncertainty at a defined point; it does not replace supplier process control or the product specification.

20. List Shipping and Document Requirements

Tell the supplier when goods may be handed over and which shipping instructions must be followed. Record forwarder contacts, booking responsibility, cargo-ready notice, pickup address, carton and pallet data, dangerous-goods status where relevant, and any consolidation plan.

Use the China Shipping Documents Checklist to check the commercial invoice, packing list, transport document, origin document, certificates, and destination-specific records before originals or final files are released.

If several suppliers share one shipment, coordinate cutoffs and receiving records with the China Shipping Consolidation Checklist .

21. Resolve Exceptions Before Issuing the PO

Create an exception list for every difference between the final requirement and the supplier’s quotation, standard process, sample, or capability. Examples include an unavailable material, changed tolerance, substituted component, packaging limit, delayed test, or incomplete certificate.

For each exception, record the requirement, supplier proposal, technical and commercial effect, evidence reviewed, decision, approver, and expiry or affected quantity. An accepted exception should be narrow and traceable; it should not silently become the standard for later orders.

If a critical exception is still open, place the affected activity on hold. A note saying to be confirmed is useful only when it also says who confirms it, by when, and whether the supplier may order material, make tooling, print packaging, or start production in the meantime.

22. Make Special Instructions Specific and Testable

Use special instructions for requirements that do not fit cleanly into a line item or attachment, such as segregation, lot coding, retention samples, photo evidence, handling limits, or a customer-specific shipping mark. Write each instruction as an action with an observable result.

Avoid broad statements such as supplier responsible for all quality or no changes allowed under any circumstances. Define what needs approval, which channel counts as written approval, who has authority, and what records the supplier must keep.

Check whether an instruction changes cost, lead time, compliance, packaging, or inspection. If it does, update the affected PO field and attachment as well. A special note should not contradict the price table, specification, or delivery schedule.

23. Create a Controlled Attachment List

Add an attachment register to the PO. Typical entries include the final quotation, product specification, drawing, bill of materials, sample approval, color standard, packaging specification, artwork, label file, inspection plan, test requirement, shipping instruction, and approved exception list.

For every attachment, record the document title, number, revision, date, owner, and approval status. Use file names that match the register. If a cloud link is used, confirm the supplier can access the controlled version and cannot mistake an editable working file for an approval.

Package the PO and attachments together for release. Ask the supplier to acknowledge the complete set instead of signing only the first page. When a file is replaced, preserve the previous version in the order history and update the register.

Controlled attachment register
DocumentRevision and dateStatusSupplier confirmation
Product specificationDocument number, revision, issue dateApproved or open hold pointName and date
Artwork and packagingFile name, revision, approval dateProof approved or pendingName and date
Inspection planPlan number and revisionApplicable to this POName and date
Exception listRevision and decision dateAccepted, rejected, or openName and date
The PO should point to one identifiable version of every supporting document.

24. Control Purchase Order Revisions

Assign a new revision whenever an approved PO field or referenced attachment changes. Show the revision code, date, author, approver, and concise change summary. Do not overwrite the prior PDF and keep the same file name without a revision marker.

Send the revised PO through the agreed channel and state which version it supersedes. Ask the supplier to stop using earlier versions, confirm receipt, assess cost and schedule impact, and return acceptance. Update finance, quality, and logistics when the change affects their records.

Distinguish corrections from commercial changes. Fixing a typing error may not alter supplier obligations, while changing a material or delivery date may require price, testing, tooling, and payment updates. The revision history should make that difference visible.

25. Use a Written Change-Order Process

After production release, route proposed changes through a change-order record rather than informal chat approval. The request should describe the current requirement, proposed change, reason, affected quantity, inventory or work already completed, and requested decision date.

Require the supplier to assess price, lead time, tooling, quality, compliance, packaging, inspection, and shipping effects. The buyer then accepts, rejects, or modifies the proposal through an authorized approver. No affected work should continue when the change creates an unresolved critical risk.

Once approved, update the PO and every affected attachment. Record disposal, rework, or acceptance of existing material. This prevents the change record from becoming a separate instruction that later conflicts with the specification or inspection criteria.

26. Obtain Supplier Confirmation

Ask an authorized supplier representative to confirm the PO number and revision, complete attachment list, product and quantity, price and currency, production start condition, milestones, Incoterm, payment terms, inspection requirements, and open exceptions.

A signature or company stamp can support the record, but it is not a substitute for checking whether the signer has authority or whether the parties agree on document priority. For significant orders, align the acceptance method with the governing commercial agreement and legal advice.

Do not treat silence or a casual received message as operational acceptance. Ask the supplier to identify anything it cannot meet and return a dated confirmation. Keep the reply in the order file alongside the exact PO package it covers.

27. Release Production Only After Conditions Are Closed

Create a production-release gate. The buyer’s authorized owner should confirm that the PO, specification, sample status, packaging, artwork, price, payment approval, milestones, inspection plan, and supplier acceptance are complete enough for the next activity.

Separate authorization to buy material, make tooling, print packaging, run a pilot, and begin mass production when the risks differ. This lets the project move in controlled stages without implying that every unresolved item has been accepted.

Record the release date, scope, approver, conditions, and evidence. If release is conditional, name the hold point and prohibited activities. The supplier should not infer mass-production approval from a sample payment, deposit, artwork discussion, or shipping forecast.

28. Keep a Complete Order File

Store the issued PO, revisions, supplier confirmations, quotations, PI, specifications, samples, artwork approvals, exceptions, payment records, production updates, inspection reports, corrective actions, and shipping documents under the same order reference.

Make the current version easy to find while preserving the history. Access should be controlled, but finance, quality, logistics, and management need the records required for their decisions. Keep significant approvals out of private chat accounts where the business cannot retrieve them.

Close the file with final quantities, total payments, credits, defects, claims, shipment references, and lessons for the next order. A clear closeout helps the buyer prepare repeat orders without copying an old mistake or losing an approved improvement.

29. Avoid Common Purchase Order Mistakes

Common failures include issuing the PO to the wrong entity, using an outdated quotation, combining variants under a vague description, omitting price inclusions, writing an incomplete named place, and leaving sample or artwork versions unidentified. Each one creates room for two reasonable but different interpretations.

Other problems appear after release: changes approved in chat, payments disconnected from milestones, inspection booked too late, revised files sent without a change summary, or production started before supplier confirmation. These are control failures, not formatting problems.

A longer PO is not automatically better. Remove repeated boilerplate that conflicts with the actual order, and move technical detail into controlled attachments. The useful test is whether a new colleague and the supplier can reach the same answer about product, money, timing, quality, and handover.

30. Run the Final Purchase Order Review

Before sending the PO, read it once as the supplier’s production team, once as the buyer’s finance reviewer, and once as the inspector. Each reader should be able to identify the order, current documents, required action, approval authority, deadline, and evidence without searching through negotiation history.

Then use the structured checklist below. Mark each item complete, not applicable with a reason, or open with an owner and deadline. Stop release when an open item could change product acceptance, legal entity, price, payment safety, tooling, compliance, or a critical delivery date.

Finally, send one controlled package, obtain supplier confirmation, and record the exact scope of production release. The objective is not a perfect form. It is a shared, traceable order baseline that gives the buyer and supplier a practical way to manage questions and changes.

01

Buyer and Supplier

Confirm who is issuing, accepting, operating, and approving the order.

  • Buyer legal name and address are complete.
  • Supplier legal name and address match verified records.
  • Any exporter, trading company, factory, or payment entity relationship is documented.
  • Buyer and supplier operational contacts are listed by role.
  • Approval authority is clear on both sides.
02

Purchase Order Control

Give the order one controlled identity and current version.

  • PO number is unique.
  • Issue date and revision are shown.
  • Buyer project and supplier quotation references are included.
  • Order owner and status appear in the PO register.
  • Earlier revisions can be retrieved but are not mistaken for current.
03

Quotation and Pricing

Reconcile the PO to the commercial basis the buyer approved.

  • Approved quotation or PI number, date, and revision are referenced.
  • Unit price, currency, line totals, and grand total are correct.
  • One-time fees, credits, and adjustments are separate.
  • Price inclusions and exclusions are explicit.
  • Open estimates have an approval rule and evidence requirement.
04

Product Identification

Make every ordered item and variant unambiguous.

  • Buyer SKU and supplier model are recorded where available.
  • Each size, color, material, voltage, language, and pack variant has its own line.
  • Quantity and unit of measure are defined.
  • Variant subtotals match the order total.
  • Substitution and quantity-variance rules are stated.
05

Specifications and Samples

Connect production to measurable requirements and approved references.

  • Final specification number, revision, and date are listed.
  • Materials, dimensions, tolerances, performance, finish, and tests are defined as applicable.
  • Approved sample ID, scope, date, photographs, and location are recorded.
  • Sample deviations and required production corrections are documented.
  • Critical open requirements remain release hold points.
06

Packaging and Branding

Control protection, pack configuration, artwork, and market-facing information.

  • Unit, inner, master-carton, and pallet requirements are defined.
  • Pack quantity, orientation, dimensions, and weight limits are stated.
  • Artwork, logo, label, barcode, warning, insert, and carton-mark files are revision controlled.
  • Required proof or pre-production approval is identified.
  • Destination-market label and claim responsibilities have been reviewed.
07

Accessories and Components

Account for everything delivered with or supporting the product.

  • Accessory and component quantities per unit are listed.
  • Compatibility and technical references are defined.
  • Spare units or parts are separate order lines.
  • Spare pricing and packing method are clear.
  • Customer-supplied or multi-source components have an owner and delivery plan.
08

Production and Delivery

Turn lead time into dated, owned milestones.

  • The exact lead-time start event is defined.
  • Material, production, packing, inspection, and handover dates are recorded.
  • Buyer-dependent approval dates are included.
  • Each milestone has an owner and evidence requirement.
  • Delay escalation and schedule revision method are agreed.
09

Incoterm and Logistics

Define the commercial handover and shipping responsibilities.

  • Incoterm rule and version are stated.
  • Named place, port, terminal, or destination is precise.
  • Export, inland transport, loading, freight, insurance, import, and delivery tasks are allocated.
  • Cargo-ready notice and forwarder instructions are defined.
  • Consolidation requirements are included where applicable.
10

Payment

Connect each amount to verified instructions and an approved condition.

  • Currency, percentage or amount, and timing are correct.
  • Deposit, prior payments, credits, fees, and remaining balance reconcile.
  • Beneficiary differences and bank changes require independent verification.
  • Each payment stage has evidence and an authorized approver.
  • Payment terms align with the PO, PI, and governing agreement.
11

Quality and Inspection

Define how conformity will be checked before release.

  • Inspection and test stages are selected.
  • Specification, method, sample size, defect classes, and acceptance criteria are referenced.
  • Inspection timing, location, access, and packing status are defined.
  • Corrective-action and exception approval paths are clear.
  • Shipment and balance release conditions reflect inspection decisions.
12

Attachments

Issue a complete and controlled supporting document set.

  • Attachment register lists title, number, revision, date, and status.
  • Specification, drawings, sample approval, packaging, artwork, inspection, and exceptions are included as applicable.
  • Supplier can access the controlled files.
  • Cloud links do not point to uncontrolled working versions.
  • Replaced files remain in the order history.
13

Supplier Confirmation

Obtain a dated acceptance of the exact order package.

  • Authorized supplier representative is identified.
  • PO number, revision, and attachment set are acknowledged.
  • Product, quantity, price, timing, Incoterm, payment, and inspection terms are confirmed.
  • Supplier has disclosed anything it cannot meet.
  • Confirmation is stored with the PO package it covers.
14

Production Release

Authorize only the work whose prerequisites are closed.

  • PO and supplier confirmation are complete.
  • Specifications, samples, packaging, artwork, and exceptions are approved to the required stage.
  • Commercial, payment, schedule, and inspection controls are ready.
  • Material, tooling, printing, pilot, and mass-production permissions are separated where needed.
  • Release scope, date, approver, conditions, and hold points are recorded.

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Need Help Turning Supplier Quotes and Product Details Into a Clear Purchase Order?

Kelsy can help organize product specifications, packaging requirements, payment milestones, supplier confirmations, and production handoff details before an order begins.

Requirement organization Connect quotations, specifications, samples, packaging files, and exceptions to the correct PO revision.
Supplier confirmation Turn open questions and supplier responses into dated, reviewable order records.
Production handoff Define release conditions, milestones, inspection evidence, and change controls before work begins.
Complete order file Keep approvals, revisions, payment records, quality decisions, and shipping documents under one reference.

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