TCVN TIEU CHUAN QUOC GIA TCVN ISO/IEC 17025:2017 ISOMEC 17025:2017 Xuat ban lan 3 YEU CAU CHUNG VE NANG LUC CUA CAC PHONG THU’ NGHIEM VA HIEU CHUAN General requirements for the competence of testing and calibration laboratories HA NOI - 2017TCVN ISO/EC 17025:2017 Muc luc Lai néi dau. Loi gidi thigu.... 1 2 3 4 Phu Ive A (tham khdo) Lién két chuan do lwéng Phy Iyc B (tham khdo) Cc la chon ddl voi hg théng quan I. Thu myc tai ligu tham khéo.. Pham vi ap dung Tai ligu vién dan.. ‘Thuét ng@ va dinh nghia ‘Yéu cau chung... 4.1. Tinh khéich quan 42 Bao mét... ‘Yeu cau vé co cdu.. Yéu cau vé nguén lye. 6.1 Yéu cdu chung 6.2 Nhén sy 6.3 Co sé vat chat va diéu kin mdi trerdng ... 6.4 Thiét bj 6.5 Lién két chuan do luong 6.6 San phdm va dich vy do bén ngoai cung cdp_ Yéu cau vé qué trinh.. 7.4 Xem xét yéu cau, d8 nghi thu va hop dng 7.2 Lua chon, kiém tra xéc nhan va xac nhn gid trj si’ dyng cla phueng phap 7.3 Ldy ma 7.4 Xie ly déi twgng thir nghiém hode higu chuas 7.5 HO so ky thuat. 7.6 Banh gia 66 khong dam bao do. 7.7 Bam bao gia tri sir dung cla két qua. 7.8 Bao cdo kat qua.. 7.9 Khiéu nai.. 7.40 Céng viée khéng phit hop ... 7.11. Kidm soat dtr ligu — Quan ty thong ti Yéu cau hé thong quan ly. 81 Cac lya chon... 8.2 Tailigu hé théng quan ly (Luva chon A).. 8.3 Kiém soat tai liu hé théng quan ly (Lya chon A) 8.4 Kiém sot hd so ( Lira chon A).. 8.5 Hanh dGng dé gidi quyét ri ro va co’ hgi (Lya chon A} 8.6 Caitién (La chon A) 8.7 Hanh dong khde phyc (Lyra chon A). 8.8 Banh gid ngi bd (Lya chon A) 8.9 Xem xét ctia Idinh dao (Lyra chon A)..TCVN ISONEC 17025:2017 Table of content Foreword Introduction 1 Scope. 2 Normative references. 3 Terms and definitions . 4 General requirements.. 4.1 Impartiality. 42 Confidentiality Structural requirements 6 Resource requirements. 6.1 General. 6.2 Personnel . 6.3 Facilities and environmental conditions 64 Equipment. 6.5 Metrological traceability... 6.6 Externally provided products and services... 7 Process requirements. 7.1. Review of requests, tenders and contracts 7.2 Selection, verification and validation of methods 7.3 Sampling... 7.4 Handing of test or calibration items. 7.5 Technical records 7.8 Evaluation of measurement uncertaint 7.7 Ensuring the validity of results... 7.8 Reporting of results 7.8 Complaints 7.10 Nonconforming work... 7.11 Control of data — Information management 8 Management system requirements. 8.1. Options... 8.2 Management system documentation (Option A) 8.3 Control of management system documents (Option A). 8.4 Control of records (Option A) 8.6 Improvement (Option A) 8.7 Corrective action (Option A).. 8.8 Internal audits (Option A) 8.9 Management reviews (Option A). Annex A (informative) Metrological traceabilty.. Annex B (informative) Management System Option Bibliography a