| Sample Traceability | Sample identification code, production date or lot, package type, wafer or assembly location, and applicable datasheet revision. | Match the physical marking, packing label, certificate of analysis, and datasheet before electrical testing. | 100% of submitted samples must be traceable to a defined manufacturing lot and documented product revision. | Pass: complete and consistent records. |
| Visual and Mechanical Inspection | Package dimensions, lead or terminal finish, marking quality, polarity indication, lens or window condition, and mounting interface. | Inspect with calibrated measuring equipment and compare against the approved mechanical drawing. | No cracks, delamination, bent terminals, illegible markings, contamination, or dimensional deviations outside the drawing tolerance. | Hold: any unexplained deviation requires corrective action. |
| Forward Voltage (VF) | VF at the specified forward current and ambient temperature. | Use a calibrated source-measure unit or curve tracer. Record test current, temperature, and measurement uncertainty. | Measured values must remain within the approved datasheet limit and agreed production tolerance at the application current. | Pass: stable distribution with no outliers beyond specification. |
| Reverse Leakage (IR) | Reverse leakage current at the specified reverse voltage and temperature. | Apply the rated test voltage using current-limited equipment after allowing the device to reach thermal equilibrium. | IR must not exceed the maximum datasheet value; high-temperature results must be evaluated separately because leakage generally increases with temperature. | Review: unexplained lot-to-lot drift indicates process risk. |
| Reverse Breakdown Voltage (VBR) | Breakdown voltage distribution and test current used to define the result. | Perform a controlled voltage sweep with current limiting and record the breakdown criterion. | VBR must exceed the application maximum reverse voltage with the agreed design margin and remain within the specified range. | Pass: adequate electrical margin and repeatable distribution. |
| Capacitance and Frequency Response | Junction capacitance at the specified reverse bias, frequency, and temperature. | Measure with an LCR meter or impedance analyzer using open, short, and fixture compensation. | Capacitance must remain within the application limit at the operating frequency and bias; test conditions must be identical for all suppliers. | Review: excessive capacitance can reduce sensor bandwidth and signal accuracy. |
| Response and Recovery Performance | Rise time, fall time, reverse-recovery time where applicable, spectral response, and output repeatability. | Use the intended optical or electrical stimulus, a calibrated receiver or oscilloscope, and a controlled ambient-light condition. | Results must meet the application response-time and sensitivity limits across the specified operating temperature range. | Pass: repeatable response with no abnormal saturation or waveform distortion. |
| Temperature Performance | Electrical parameters at the minimum, room, and maximum rated operating temperatures. | Use a calibrated thermal chamber and allow sufficient stabilization before each measurement point. | All critical parameters must remain within the approved operating limits from the application temperature range, including the stated derating requirements. | Pass: no functional loss or permanent parameter shift. |
| Reliability Screening | Evidence of temperature cycling, high-temperature operating life, humidity exposure, solderability, and mechanical stress testing. | Review test plans, sample sizes, test duration, failure criteria, pre- and post-test measurements, and laboratory accreditation. | Test methods must be appropriate for the package and product type; zero catastrophic failures are required in qualification samples unless a documented reliability model supports another criterion. | Review: missing raw data is not equivalent to a passed test. |
| Change Control | Formal process for notifying changes to materials, die, package, test site, manufacturing location, or process parameters. | Check the supplier change-notification procedure and require written notice before implementation. | Advance notification should cover any change that may affect form, fit, function, reliability, compliance, or traceability. | Pass: documented notification and requalification rules. |
| RoHS Compliance | Declaration of conformity and material information for restricted substances under Directive 2011/65/EU and applicable amendments. | Review the declaration, homogeneous-material data, and test reports from a competent laboratory when required. | Documentation must cover the exact part number, package, revision, and applicable exemptions, if any. | Pass: current and product-specific evidence. |
| REACH and Substance Disclosure | SVHC communication statement and material disclosure for the applicable supply chain and destination market. | Check the declaration date, product scope, threshold basis, and update process against the latest applicable requirements. | Supplier must provide current information and notify the buyer when regulatory substance status changes. | Hold: generic or undated declarations require clarification. |
| Quality Management | Valid quality-management certification, scope, certificate expiry date, manufacturing site, and audit status. | Verify the certificate with the issuing certification body and confirm that the listed site covers the supplied product. | Certification must be valid, site-specific, and relevant to design, manufacturing, testing, or distribution activities performed. | Pass: certificate scope matches the actual supply chain. |
| Production Consistency | Historical capability data for critical parameters such as VF, IR, VBR, capacitance, and sensitivity. | Review control charts, lot acceptance records, nonconformance trends, and sampling plans. | Critical characteristics must have defined limits, recorded results, and a documented reaction plan for out-of-control conditions. | Pass: stable process evidence over multiple lots. |
| Packaging and Shipping | Moisture sensitivity information, dry-pack method where applicable, storage conditions, shelf life, and label format. | Inspect packaging integrity and compare the shipping documents with the receiving inspection requirements. | Packaging must protect against moisture, electrostatic discharge, contamination, and mechanical damage throughout the planned transport route. | Review: damaged or incomplete packaging can compromise otherwise good samples. |
| Capacity and Lead Time | Monthly capacity, standard lead time, minimum order quantity, forecast flexibility, and allocation policy. | Compare documented capacity with the forecast, ramp plan, and required safety-stock level. | Supplier should demonstrate capacity for normal demand plus the agreed peak requirement without compromising inspection or traceability. | Pass: capacity assumptions are documented and testable. |
| Long-Term Technical Support | Named technical contact, failure-analysis process, response-time commitment, test-report format, and product-lifecycle policy. | Run a technical inquiry and record response completeness, turnaround time, and ability to provide corrective-action evidence. | Routine technical questions should receive a defined response within 3 business days; critical quality incidents require an agreed containment and corrective-action timeline. | Pass: support is measurable, documented, and maintained after approval. |
| Commercial and Supply Risk | Quotation validity, payment terms, tooling ownership, warranty terms, alternate manufacturing-site policy, and business-continuity plan. | Review the supply agreement and confirm responsibilities for shortages, obsolete parts, recalls, and nonconforming material. | Commercial terms must define quality responsibility, notice periods, escalation routes, and recovery actions for supply interruption. | Review: unclear liability or continuity planning increases total sourcing risk. |
| Final Supplier Score | Weighted results from sample verification, testing, compliance, quality systems, capacity, and support. | Score each category using the same evidence requirements and retain the completed evaluation record. | Recommended gate: technical and compliance items must pass; overall score at least 80/100; no unresolved critical nonconformity. | Approve: qualified for controlled production sourcing. |