Skill Packages
Browse ready-made AI workflow skills for document elaboration, review, and structuring.
ISO 17025 Management Review
Prepare and conduct management reviews per ISO/IEC 17025:2017 Clause 8.9. Compiles all required inputs (internal audits, corrective actions, PT results, risk assessments, resource adequacy), documents review decisions, and tracks action items. Review input validator checks all Clause 8.9.2 categories; action item tracker validates decisions, owners, and deadlines.
Learn MoreISO 17025 Measurement Uncertainty
Estimate measurement uncertainty per ISO/IEC 17025:2017 Clause 7.6 using GUM (JCGM 100:2008) methodology. Builds uncertainty budgets with Type A/B component identification, distribution divisors, sensitivity coefficients, law of propagation of uncertainty, Welch-Satterthwaite for effective degrees of freedom, and coverage factor justification per ILAC P14:01/2020. Validates budget completeness and Clause 7.8.3/7.8.4 reporting compliance including decision rules and guard-band methods for conformity statements.
ISO 17025 Method Selection, Verification & Validation
Build and validate method selection, verification, and full/partial validation procedures per ISO/IEC 17025:2017 Clause 7.2. Covers the Clause 7.2.1.1 method selection hierarchy, verification of standard methods, partial validation for deviated standard methods (Cl.7.2.1.4), and full validation of non-standard/lab-developed methods with track-aware performance characteristics, CRM/reference material strategy, acceptance criteria, and fitness-for-purpose conclusions. Extension tools validate protocol completeness and report compliance with track-aware minimum characteristic counts.
ISO 17025 Metrological Traceability
Establish and validate metrological traceability per ISO/IEC 17025:2017 Clause 6.5. Documents traceability chains from working standards through reference standards to NMI/SI for each measurand. Manages reference standards and certified reference materials (CRMs) with certificates, expiry tracking, and storage conditions. Extension tools validate chain completeness and reference standard register entries.
Learn MoreISO 17025 Personnel Competence
Personnel competence management per ISO/IEC 17025:2017 Clause 6.2. Builds competence matrix mapping personnel to authorized methods, documents training programs, and ensures business continuity through redundant authorization. Competence matrix validator checks completeness; authorization coverage checker flags single-point-of-failure methods.
Learn MoreISO 17025 Quality Manual & Document Control
Draft and validate quality management system documentation per ISO/IEC 17025:2017 Clauses 8.1–8.4. Produces a quality manual with quality policy, document control procedure, record control procedure, and master document list. Quality manual checker validates policy, structure, and clause coverage; document control validator ensures approval, revision, and distribution processes are defined.
Learn MoreISO 17025 Reporting of Results
Design and validate test reports and calibration certificates per ISO/IEC 17025:2017 Clause 7.8. Creates compliant report templates with all mandatory elements (title, lab ID, unique reference, customer info, method, dates, results with units, signatures), handles opinions/interpretations per Clause 7.8.7, defines decision rules for conformity statements per Clause 7.8.6, and establishes amendment procedures.
Learn MoreISO 17025 Request, Tender & Contract Review
Build and validate a procedure for reviewing requests, tenders, and contracts per ISO/IEC 17025:2017 Clause 7.1. Ensures the laboratory confirms capability, selects appropriate methods, and communicates with customers before accepting work. Covers new and repeat requests, amendments, subcontracting decisions, and dispute resolution. Extension tool validates completeness of all required procedural elements.
Learn MoreISO 17025 Risk, Opportunity & Corrective Action Management
Identify and manage laboratory risks and opportunities per ISO/IEC 17025:2017 Clauses 8.5–8.7. Produces a scored risk register, corrective action procedure with root cause analysis, and CAPA tracking log. Risk register validator checks entry completeness and scoring; corrective action tracker validates procedure elements from trigger through effectiveness verification.
Learn MoreISO 17025 Sampling & Test Item Handling
Build and validate sampling plans (Clause 7.3) and test/calibration item handling procedures (Clause 7.4) per ISO/IEC 17025:2017. Covers sampling methodology with statistical basis, sample receipt and registration, unique identification systems, condition assessment, handling to prevent damage and contamination, storage conditions, preparation, retention, and disposal. Extension tools validate sampling plan completeness and item handling procedure compliance.
Learn MoreISO 17025 Technical Records
Establish technical records and data management procedures per ISO/IEC 17025:2017 Clauses 7.5 and 7.11. Covers recording requirements (date, personnel, equipment, conditions, observations, calculations), correction procedures (single-line strike), original observation preservation, data integrity controls, LIMS/software validation, electronic record management with audit trails, and data retention policies.
Learn MoreISO 17025 Validity of Results
Design and validate a quality assurance program per ISO/IEC 17025:2017 Clause 7.7. Covers internal QC techniques (CRMs, replicates, spikes, blanks), proficiency testing and inter-laboratory comparisons, control chart monitoring (Shewhart, CUSUM), out-of-control response procedures, and performance evaluation using z-scores and En numbers. Validates QC program completeness and PT/ILC coverage for all accredited methods.
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