1.ПК 01-09.02 СМ. Quality policy and objectives ed. 16 from 17.05.2023 y.
2.П 01-07.04 СМ. Policy in the field of traceability of measurement results change. 1 ed.7 from 20.01.2023 y.
3.П 01-07.05 СМ. Policy on participation in activities in the field of qualification verification ed.6 from 27.12.2021 y.
4.ПС 01-04.06 СМ. Regulations on the Accreditation Development Committee change.1 ed.4 from 17.11.2022 y.
5.П 01-07.07 СМ. Cross-border accreditation policy ed.2 from 02.02.2022 y.
6.П 01-07.09 СМ. Policy on uncertainty of measurement results ed. 3 from 27.12.2021 y.
7.П 01-07.10 СМ. Politics. Application of GOST ISO/IEC 17020 for accreditation of inspection bodies" ed.2 from 27.12.2021 y.
8.П 01-07.11 СМ. Policy on the transition to ST RK ISO 50003-2022 ed.1 from 11.05.2023 y.
9.П 01-04.13 СМ.Impartiality policy ed.4 from 17.05.2023 y.
10.П 01-07.14 СМ. Policy on transition to ST RK ISO 14064-1-2019, ST RK ISO 14064-2-2019, ST RK ISO 14064-3-2019, ST RK ISO/IEC 17029-2020 P 01-07.14 ed.2 from 27.12.2021 y.
11.П 01-07.19 "СМ. Policy on transition to electronic accreditation of subjects in the field of conformity assessment (e-Accreditation)" ed. 3 from 03.03.2022 y.
12.ДП 02-07.07 СМ. Appeals change.1 к ed. 5 from 04.05.2023 y.
13.ДП 02-08.09 СМ. The process of monitoring the compliance of testing centers with the principles of good laboratory practice ed.1 from 22.10.2022 y.
14.ПП 02-05.10 СМ. Regulations on technical committees for accreditation of conformity assessment bodies ed.2 from 30.12.2021 y.
15.ДП 02-07.15 СМ. Accreditation process change.3 ed. 8 from 24.05.2023 y.
16.ДП 02-07.16 СМ. Re-accreditation and planned evaluation change.1 ed. 8 from 17.11.2022 y.
17.ДП 02-07.17 СМ.Suspension, revocation, termination and renewal of the accreditation certificate ed. 7 from 12.10.2022 y.
18.ДП 02-04.18 СМ. Accreditation mark change.3 ed. 4 from 24.05.2023 y.
19.ДП 02-04.19 СМ. Expansion of NCA activities change.1 ed. 4 from 30.01.2023 y.
20.ДП 02-07.20 СМ. Renewal of the accreditation certificate ed. 5 from 11.02.2022 y.
21.ДП 02-07.21 СМ. Updating of accreditation materials ed.11 from 28.04.2023 y.
22.ДП 02-05.27 СМ. Consideration of complaints change.1 ed.7 from 26.05.2023 y.
23.ДП 02-07.28 СМ. Expansion or reduction of the scope of accreditation of accredited entities change.1 к ed.5 from 20.01.2023 y.
24.ДП 02-04.30 CМ. Laboratory combined MRA sign. References to accreditation change.1 ed.5 from 26.05.2023 y.
25.ДП 02-04.32 СМ. Combined IAF MLA Sign. References to accreditation change.1 ed.4 from 26.05.2023 y.
26.РИ 03-07.04 СМ.The accreditation process. Witness assessment for OPS SEE change.2 ed.2 from 11.05.2023 y.
27.РИ 03-07.09 СМ. The accreditation process. Application review and resource analysis change.1 к ed.13 from 11.05.2023 y.
28.РИ 03-07.11 СМ.The accreditation process. Examination of a set of documents change.2 к ed. 9 from 01.03.2023 y.
29.РИ 03-07.12 СМ.The accreditation process. Examination by location change.1 ed.8 from 29.11.2022 y.
30.РИ 03-07.12 ОПС СМ.The accreditation process.Survey at the location of the OPS change.2 ed.7 from 01.03.2023 y.
31.РИ 03-07.13 СМ. Expression and estimation of uncertainty of measurement results ed.2 from 29.12.2021 y.
32.РИ 03-07.14 СМ. The accreditation process. Application of the results of the qualification test in the evaluation of laboratories change.1 ed.5 from 15.11.2022 y.
33.РИ 03-07.20 Requirements for the design and content of the accreditation certificate ed.4 from 11.02.2022 y.
34.РИ 03-07.23 СМ. The accreditation process. Witness assessment in the evaluation of laboratories (centers) ed.2 from 31.03.2022 y.
35.РИ 03-07.26 СМ. СМ.The procedure for maintaining the national part of the Unified Register of Conformity Assessment Bodies of the Eurasian Economic Union ed.3 from 27.12.2021 y.
36.РИ 03-07.33 СМ. The accreditation process. Witness assessment during the evaluation of the OPS PiU change.1 ed.2 from 26.12.2022 y.
37.РИ 03-07.34 СМ.The accreditation process. Remote assessment change.1 ed.2 from 13.02.2023 y.
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