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Appendix 1 — Method Register

Parent procedure: 10 – Test and Calibration Methods

Purpose

To provide a single, controlled reference for all test and calibration methods approved for use in the laboratory. The register records the method source, scope, verification or validation status, linked SOP, and review history. It is the definitive list of what the laboratory is authorized to perform.

Instructions

  1. The Technical Manager adds a new entry when a method is approved for routine use, following successful verification or validation.
  2. The register is reviewed at least annually to confirm that SOP revisions, standard edition references, and verification/validation status are current.
  3. Methods that are retired or superseded are moved to Part B.
  4. This register is a controlled document managed per Procedure 00.

Part A — Active Methods

Complete one row per method. Where a single SOP covers multiple analytes (e.g., a multi-element ICP-OES method), use a single row and list all analytes in the "Analyte / Measurand" column.

Method IDMethod nameAnalyte / MeasurandMatrix / ScopeMethod typeReference standard or sourceSOP number (current revision)Verification / Validation statusDate verified / validatedNext review dueTechnical Manager sign-off
M-001ICP-OES multi-element analysisNi, Co, Mn, Li, Al, FeNMC/NCA/LCO cathode powders; acid digestIn-houseLaboratory developmentSOP-10-001 Rev. 02Validated — Report VAL-001[Date][Date][Initials]
M-002Karl Fischer moisture determinationMoisture (H₂O)Cathode and anode active materialsStandardISO 760:[year]SOP-10-002 Rev. 01Verified — Record VER-002[Date][Date][Initials]
M-003Laser diffraction particle size distributionD10, D50, D90, spanCathode and anode powders, wet dispersionStandardISO 13320:[year]SOP-10-003 Rev. 01Verified — Record VER-003[Date][Date][Initials]
M-004BET specific surface areaBET surface area (m²/g)Cathode and anode active materialsStandardISO 9277:[year]SOP-10-004 Rev. 01Verified — Record VER-004[Date][Date][Initials]
M-005HPLC-UV organic impurity analysisNMP, PVDF, other organic impuritiesAnode material extractsIn-houseLaboratory developmentSOP-10-005 Rev. 01Validated — Report VAL-005[Date][Date][Initials]
[Add rows]

Method type key: Standard = published standard method used within scope · Modified = standard method adapted beyond original scope · In-house = laboratory-developed method


Part B — Method Deviations Log

Record all authorized temporary deviations from active methods. This log is reviewed by the Technical Manager quarterly.

Deviation ref.Method IDDeviation descriptionBatch / Sample ref.Technical justificationAuthorized byDateDisclosed on report?Follow-up action
DEV-001M-001Modified acid ratio for high-Fe samples showing incomplete dissolution with standard 3:1 HNO₃:HCl mixture[Batch ref.]High Fe content (>15%) caused incomplete dissolution; 4:1 ratio confirmed by dissolution check[Name][Date]Yes — noted on reportReview SOP for high-Fe scope; consider method extension
[Add rows]

Part C — Retired Methods

Record methods that are no longer in active use. Records are retained per Procedure 00.

Method IDMethod nameDate retiredReasonSOP archived atRecords retained until
[ID][Name][Date][e.g., Superseded by M-006, customer no longer requires][Archive ref.][Date]

Part D — Standard Method Edition Tracking

Record the publication date of standard methods in use and document the outcome of reviews when new editions are published.

Method IDStandard referenceEdition in useLatest published editionReview dateReview outcomeAction takenReviewed by
M-002ISO 760[year][year][Date][e.g., No technical changes — no re-verification required / Technical changes — re-verification required][e.g., SOP updated to reference new edition][Name]
M-003ISO 13320[year][year][Date]
M-004ISO 9277[year][year][Date]
[Add rows]

Register maintained by: [Technical Manager name]Last reviewed: [Date]

:::tip Adapt this template Pre-populate Part A with your laboratory's actual methods. The sample entries reflect the battery materials laboratory scope. If your laboratory uses a LIMS or document management system that tracks method status, this register may be generated from that system — but a controlled, reviewable version must always be available for assessment purposes. :::