“Approved as sample” is not a usable production instruction until the sample, drawings, configuration, exceptions and authorised decision are tied to one controlled record.
A sample window sits in a meeting room. The colour looks right, the handle turns and someone writes “approved” in a message. Weeks later, production asks which glass spacer was accepted, whether the drainage detail was reviewed and whether the sample represented appearance or performance. The object did not fail; the approval record did. A useful sample closes named decisions and leaves the unresolved ones visible.
Use boundary: This is a buyer-side control method, not a universal standard form. Project specifications, contracts, applicable standards and the responsible technical team govern the actual approval route.
1. Decide what question the sample must answer
Do not begin with “make a sample”. Begin with the decision that is holding the project: finish approval, sightline and operation review, hardware confirmation, glazing appearance, interface review, workmanship reference—or a combination of these.
For a wider project package, connect the sample brief to the aluminum window specification checklist and the current window schedule. A sample built against an obsolete mark or drawing revision can be beautifully made and still be irrelevant.
- Project and opening mark represented
- Purpose of the sample
- Drawing and schedule revision
- Items included and intentionally omitted
- Named reviewers and decision deadline
2. Give the sample a configuration identity
A photograph is useful evidence of condition, but it does not identify hidden build-up or later substitutions. Assign a sample reference and record the proposed frame, sash, mullion or track route; dimensions and operation; glass build-up; spacer; finish; hardware; gaskets and seals; drainage features; screen; and included accessories.
Photograph the whole unit, corners, drainage, hardware, labels and any approved visual reference under agreed viewing conditions. Keep a retained physical sample, cut section or signed colour/glass reference when practical. The National Glass Association glazing manual specifically advises retaining mock-up glass for future reference; that makes the reference retrievable when later visual questions arise.
| Record field | What to enter | Why it matters |
|---|---|---|
| Sample ID | Project code + opening mark + revision | Stops one sample being confused with another |
| Controlled inputs | Drawing, schedule, finish and hardware revisions | Shows what the fabricator actually followed |
| Configuration | System, size, operation, glass, spacer, finish, hardware, seals and screen | Makes “as sample” technically retrievable |
| Visual evidence | Dated overview and detail photographs; retained references where agreed | Supports later appearance comparison |
| Exceptions | Omitted, provisional or non-representative items | Prevents silence being read as approval |
3. Review the unit in a fixed sequence
Start with identity, then geometry, appearance, operation and interfaces. Jumping straight to the handle or colour makes it easy to miss that the sample was built to the wrong revision.
Operate every moving element more than once. Look for consistent engagement, clearance, rubbing, rocking or interference, but do not turn a showroom operation check into a durability claim. Review drainage paths and installation interfaces as visible design details; a dry tabletop observation is not a water-penetration test.
- Match the sample ID to the current approved review documents.
- Check overall dimensions, opening type, handing and visible geometry.
- Compare finish, glass appearance, spacer, hardware, seals, screens and accessories with the agreed references.
- Operate sash, panel, locks, restrictors and removable parts; record observations rather than vague “good quality” labels.
- Inspect corners, joints, glazing, drainage openings, fastener preparation and installation interfaces that the sample is intended to represent.
- Photograph every exception and give it an owner, disposition and due date.
4. Separate sample approval from performance evidence
An approval sample can confirm selected configuration and workmanship observations. It cannot, merely by existing, prove air leakage, water penetration, structural resistance, thermal performance, acoustic performance, safety compliance or durability.
ASTM publishes separate methods for laboratory air leakage, water penetration and structural performance of a named specimen under specified conditions. Use the test report review guide to compare that specimen and method with the proposed project unit; do not write “performance approved by sample” unless the governing project process has separate evidence for that conclusion.
| Review subject | Sample can support | Separate evidence still needed |
|---|---|---|
| Colour and visible finish | Comparison with an agreed retained reference under stated conditions | Project acceptance criteria and permitted variation |
| Operation | Observation of the sampled unit at review | Cycle, load or durability evidence where required |
| Air, water and structural performance | Confirmation of the sampled configuration details | Applicable calculation or test evidence for the proposed unit |
| Installation interface | Review of represented sections and details | Approved project detail, substrate and site execution |
| Production consistency | A controlled reference for later comparison | Inspection plan, records and change control across the order |
5. Use four decisions—not one approval stamp
A sample review should end with one of four dispositions. “Approved” means the named review scope is closed against the recorded inputs; it does not erase exclusions or replace separate technical evidence.
ISO guidance on documented information identifies specifications, work or test instructions, inspection plans and records of design inputs, controls, outputs and changes as examples of information that can support controlled processes. The practical lesson is simple: the decision must be retrievable, scoped and connected to the documents production will use.
- Approved: the recorded review scope is accepted without open changes.
- Approved with recorded comments: only when the comments are unambiguous, owned and incorporated before release.
- Revise and resubmit: the sample cannot be the production reference until the listed issues are closed.
- Rejected or wrong basis: the sample does not represent the required revision, configuration or approval purpose.
6. Close the gap between sample and mass production
Do not release production from the sample record alone. Cross-check the final drawings, window schedule, bill of quantities, configuration schedule and commercial scope. The sample may represent one critical mark while the order contains several systems, sizes, colours or hardware routes.
Use the supplier evaluation guide to examine how the supplier transfers the approved reference into purchasing, fabrication, inspection and packing records. Ask where the sample ID appears, who can authorise a substitution and how inspectors learn that a later revision replaced the retained reference.
- Approved sample record and dated photographs
- Final drawing and schedule register
- Configuration and scope matrix
- Open-evidence and exception register
- Production release authorisation
- Inspection plan tied to the approved characteristics
7. Treat every later difference as a change
A change in glass, spacer, finish batch, hardware series, gasket, reinforcement, dimensions or operation may affect appearance, interfaces, evidence or price. Do not let “equivalent” become an undocumented production decision.
Record the proposed difference, reason, affected opening marks, technical and commercial effect, supporting evidence, authorised disposition and revision date. If the change alters what the retained sample represents, update the approval record or produce a new reference. The old sample should remain identifiable as superseded rather than quietly reused.
Release question: The production question is not “Does it look close to the sample?” It is “Does this unit match the current controlled configuration, and are every authorised difference and unresolved evidence gap visible?”
8. Copy this approval record
Use one row per sample or controlled reference. Add project-specific fields rather than deleting the identity, scope, exception and authorisation controls.
| Field | Record |
|---|---|
| Project / package | [enter] |
| Sample ID / opening mark / revision | [enter] |
| Approval purpose and scope | [enter] |
| Drawings and schedules used | [enter] |
| Configuration represented | [enter] |
| Items omitted or provisional | [enter] |
| Observations and exceptions | [enter] |
| Separate evidence still open | [enter] |
| Disposition | Approved / approved with comments / revise and resubmit / rejected |
| Actions, owner and due date | [enter] |
| Authorised reviewers and date | [enter] |
| Retained sample and photo location | [enter] |
Map what each sample represents across the order
Build a coverage list before ordering sample fabrication. For each opening group, name the characteristic you want to review and the proposed reference: a finish swatch, a cut section, an operable assembly or an installation mock-up. These objects answer different questions. A colour swatch does not show sash operation; a cut section does not show how a complete unit meets an adjacent wall.
For example, an order may contain repeated casements, fixed glazing and an interior sliding partition. A casement sample might represent an agreed finish reference shared by some items, but it does not demonstrate the partition's track or the fixed unit's glazing arrangement. Record shared characteristics and unrepresented characteristics separately. The project team should decide which additional references are needed; this example does not prescribe a sample count.
Give every coverage statement a drawing or schedule reference. If a later revision changes the characteristic being reviewed, reopen that part of the coverage list. Do not silently extend approval to a new variant because its name belongs to the same product family.
Turn an approval comment into a closed action
Hypothetical review note: finish accepted; replace the provisional handle; screen not included in this sample. A single approved stamp would hide two different limitations. Record finish acceptance only against its agreed reference. Record the handle as an action requiring the named replacement and the appropriate follow-up review. Record the screen as not represented, with its separate review route.
For each action, capture the sample ID, photograph or detail reference, required response, owner and approving party. A supplier's reply that the item has been changed is not the same as the required review being closed. Attach the revised evidence and the authorised disposition so production can find the decision without searching through chat messages.
Keep the old observation visible after closure. Replacing the original note with done removes the reason for the change and makes later comparison harder. A concise closed record shows what was observed, what changed and who accepted the revised reference.
Reconcile the retained reference with the release pack
Before release, compare the sample record with the current drawing register and component schedule. Resolve any mismatch between the object retained in the meeting room and the configuration production will build. Mark a superseded reference clearly and identify its replacement; keep photographs and records linked even where storing the complete object is impractical.
Where buyer and factory retain separate references, record whether they are matched copies or different objects approved for different purposes. Agree how a disputed appearance detail will be compared. Uncontrolled phone photographs should not quietly become the only colour reference after the physical sample is packed away.
Connect the sample record to the specification checklist and the test-report review where performance evidence remains open. Discuss the sample scope with your opening schedule, the decisions to be reviewed and the variants the sample will not represent.
FAQ
Does an approved sample prove the window meets air, water or wind requirements?
No. The sample may document the represented configuration and observed workmanship, but performance conclusions require the applicable project evidence and review route.
Can photographs replace a retained sample?
Photographs help identify condition and details, but they may not reproduce colour, texture, reflectance or hidden configuration. Use retained physical references where the project needs later visual comparison, and keep the configuration record in either case.
Should a sample be approved before paying a deposit?
That depends on the commercial agreement and lead time. At minimum, the contract should state when the sample is required, what it approves, who decides, and whether production may begin before its disposition.
What happens if one component changes after approval?
Record the difference and assess its effect on appearance, interfaces, evidence, price and programme. Obtain the required authorisation and update or replace the controlled reference before production uses the change.
Can one sample represent every window in the order?
Only for the characteristics it genuinely shares. Different systems, opening types, glass, finishes, hardware or critical sizes may need separate references or clearly documented coverage.
Continue the project review
Connect this guide with the proposed window and door systems, then review how Cavorlen approaches manufacturing and quality control. When your schedule is ready, send it through the project review form.
Official sources used
ISO — Guidance on documented information for ISO 9001:2015 ↗ISO — ISO 9001 explained ↗ASTM — Building standards index for fenestration test methods ↗ASTM E331 — water penetration of exterior windows and doors ↗National Glass Association — GANA Glazing Manual ↗Related buyer guides
This guide separates configuration and workmanship approval from performance evidence. It does not certify a product, approve project engineering, replace the governing specification, or make a performance claim for Cavorlen or any supplier.