Mold Approval: Approve, Condition, or Hold

A structured buyer workspace for deciding whether the evidence supports approval, controlled conditional approval, or a hold.

Buyer-side engineering explainer

Mold Approval: Approve, Condition, or Hold

Mold approval should follow a traceable review of defects, dimensions, process stability, documentation, and every open item. A good final sample alone does not close the approval package.

PTA buyer review mode
Buyer review: connect the finding to evidence and a decision Final samples Issues register Dimensions Process record Tool documents DECISION Evidence before release Static fallback: review the full evidence package before releasing the next buyer decision.

Static review summary: approve only when required evidence is closed, approve with conditions only when controlled open items have owners and release criteria, and hold when critical risk remains unresolved.

Step 1: Receive closure package

Confirm the sample identity, cavity set, revision, process record, and issues list before reviewing sign-off.

Step 2: Review findings

Structural findings normally require closure evidence; cosmetic findings need an agreed acceptance standard or correction.

Step 3: Review dimensions

Review critical dimensions, assembly fit, and cavity-to-cavity variation rather than accepting a selected sample.

Step 4: Review stability

Ask whether the approved samples came from a repeatable, documented process under production-relevant conditions.

Step 5: Review documents

Missing ownership, maintenance, process, acceptance, or transfer documents can remain a commercial and operational risk after sign-off.

Step 6: Separate open items

Every conditional item should have an owner, due date, evidence requirement, and written release condition.

Step 7: Approval decision

Approve only when required evidence is closed; use conditions for controlled open items and hold for unresolved critical risk.

This buyer-side explainer is a review framework, not a substitute for engineering, quality, commercial, or legal approval procedures. Approval requirements should be verified against the actual program, contract, drawing, samples, tests, and supplier records.