| Stage | What ABERY Reviews or Performs | Typical Output |
|---|---|---|
| 1. Program Review | Part drawings, CAD, resin, annual forecast, quality requirements and current supply issue | Scope, open-item list and quotation inputs |
| 2. Tool & Process Review | Mold condition, ownership, dimensions, interfaces, process history and machine compatibility | Incoming-tool report and transfer plan |
| 3. Trial & Qualification | Tool setup, process window, sample run and agreed inspection | Trial report, samples and action list |
| 4. Customer Approval | Corrections, repeat trial and required submission documents | Approved sample or documented release decision |
| 5. Repeat Supply | Production scheduling, lot control, inspection, packaging and shipment release | Production records and agreed shipment documents |
| Item | Recommended Website Copy |
|---|---|
| Production MOQ | Confirmed after reviewing material, setup time, cycle, inspection and packaging. |
| Lead Time | Quoted by release after material availability, tool condition and current capacity are checked. |
| Capacity Reservation | Available under an agreed forecast, order-release rule and production plan. |
| Blanket Orders | Evaluated for stable programs with defined annual demand and release terms. |
| Buffer Stock / VMI | Available by written agreement covering forecast, stock ownership, min/max levels, release signals, storage and obsolete inventory. |
| Payment Terms | Stated in the quotation or supply agreement after commercial review. |
| Inspection | Performed to the approved drawing, control plan or inspection specification. |
| Nonconforming Product | Contained and dispositioned under the agreed quality process after responsibility and affected scope are confirmed. |
Yes, subject to an incoming review. We normally request the tool drawing or mold specification, ownership records, part drawings, resin, recent samples, maintenance history and available process or inspection records. After the mold arrives, we inspect its condition and confirm machine compatibility before scheduling a qualification trial.
The qualification plan depends on the part and customer requirements. It may include incoming mold inspection, trial setup, process review, dimensional or functional inspection, material and lot records, comparison to an approved sample, corrective actions and customer approval before repeat production.
PPAP elements can be evaluated for programs that require them. Please provide the customer-specific submission level, drawing, special characteristics, material requirements, annual volume and required forms. The exact deliverables and timing are confirmed before quotation. PPAP support does not imply IATF 16949 certification.
They are program-specific. Resin purchase quantity, changeover time, cavity count, cycle time, inspection, packaging, forecast stability and available capacity all affect MOQ and lead time. We confirm both after reviewing the mold and release plan.
These options can be considered for stable repeat programs. The agreement should define the forecast horizon, firm-order window, reserved capacity, stock ownership, min/max levels, release signals, storage period and responsibility for obsolete inventory.