{"id":324567,"date":"2024-10-19T22:30:25","date_gmt":"2024-10-19T22:30:25","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iso-iec-170252017\/"},"modified":"2024-10-25T21:06:46","modified_gmt":"2024-10-25T21:06:46","slug":"bs-en-iso-iec-170252017","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iso-iec-170252017\/","title":{"rendered":"BS EN ISO\/IEC 17025:2017"},"content":{"rendered":"
ISO\/IEC 17025:2017 specifies the general requirements for the competence, impartiality and consistent operation of laboratories. ISO\/IEC 17025:2017 is applicable to all organizations performing laboratory activities, regardless of the number of personnel. Laboratory customers, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies, and others use ISO\/IEC 17025:2017 in confirming or recognizing the competence of laboratories.<\/p>\n
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
2<\/td>\n | undefined <\/td>\n<\/tr>\n | ||||||
7<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
8<\/td>\n | Introduction <\/td>\n<\/tr>\n | ||||||
9<\/td>\n | 1 Scope 2 Normative references 3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
11<\/td>\n | 4 General requirements 4.1 Impartiality 4.2 Confidentiality <\/td>\n<\/tr>\n | ||||||
12<\/td>\n | 5 Structural requirements <\/td>\n<\/tr>\n | ||||||
13<\/td>\n | 6 Resource requirements 6.1 General 6.2 Personnel <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | 6.3 Facilities and environmental conditions 6.4 Equipment <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | 6.5 Metrological traceability 6.6 Externally provided products and services <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | 7 Process requirements 7.1 Review of requests, tenders and contracts <\/td>\n<\/tr>\n | ||||||
18<\/td>\n | 7.2 Selection, verification and validation of methods 7.2.1 Selection and verification of methods <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | 7.2.2 Validation of methods <\/td>\n<\/tr>\n | ||||||
20<\/td>\n | 7.3 Sampling 7.4 Handling of test or calibration items <\/td>\n<\/tr>\n | ||||||
21<\/td>\n | 7.5 Technical records 7.6 Evaluation of measurement uncertainty 7.7 Ensuring the validity of results <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | 7.8 Reporting of results 7.8.1 General <\/td>\n<\/tr>\n | ||||||
23<\/td>\n | 7.8.2 Common requirements for reports (test, calibration or sampling) 7.8.3 Specific requirements for test reports <\/td>\n<\/tr>\n | ||||||
24<\/td>\n | 7.8.4 Specific requirements for calibration certificates 7.8.5 Reporting sampling \u2013 specific requirements <\/td>\n<\/tr>\n | ||||||
25<\/td>\n | 7.8.6 Reporting statements of conformity 7.8.7 Reporting opinions and interpretations 7.8.8 Amendments to reports 7.9 Complaints <\/td>\n<\/tr>\n | ||||||
26<\/td>\n | 7.10 Nonconforming work <\/td>\n<\/tr>\n | ||||||
27<\/td>\n | 7.11 Control of data and information management 8 Management system requirements 8.1 Options 8.1.1 General <\/td>\n<\/tr>\n | ||||||
28<\/td>\n | 8.1.2 Option A 8.1.3 Option B 8.2 Management system documentation (Option A) 8.3 Control of management system documents (Option A) <\/td>\n<\/tr>\n | ||||||
29<\/td>\n | 8.4 Control of records (Option A) 8.5 Actions to address risks and opportunities (Option A) <\/td>\n<\/tr>\n | ||||||
30<\/td>\n | 8.6 Improvement (Option A) 8.7 Corrective actions (Option A) <\/td>\n<\/tr>\n | ||||||
31<\/td>\n | 8.8 Internal audits (Option A) 8.9 Management reviews (Option A) <\/td>\n<\/tr>\n | ||||||
33<\/td>\n | Annex A (informative) Metrological traceability <\/td>\n<\/tr>\n | ||||||
35<\/td>\n | Annex B (informative) Management system options <\/td>\n<\/tr>\n | ||||||
37<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" General requirements for the competence of testing and calibration laboratories<\/b><\/p>\n |