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CERTIFICATION

AUDISO a.s. is a certification company accredited by the Czech Accreditation Institute, o.p.s. according to ISO/IEC 17021.

We have been operating in Europe since 2005, in Italy since 2014, and we have issued approximately 5,000 certificates, which are variously distributed among different accredited standards and relevant EA (European Cooperation for Accreditation) sectors.

Non-accredited certification

UNI EN ISO 19650-1:2019

ČSN 01 0391:2013

ISDP 10003:2020

UNI ISO 10004:2019

ISO 10005:2018

UNI 11034:2003

UNI CEI 11352:2014

UNI 11381:2010

UNI 11584:2021

UNI 11760:2019

UNI 11911:2023

UNI/PdR 125:2022

ISO 13009:2015

ISO 13009:2018

ISO 13485:2016

ISO 13485:2021

EN 13549:2003

UNI EN 13816:2002

ISO 37301:2021

UNI EN ISO 14015:2022

ISO 14021:2016

ISO 14021:2021

EN 14025:2010

ISO 14040:2021

ISO 14044:2021

UNI EN ISO 14046:2016

EN 14056:2004

ČSN EN ISO 14064-2:2019

*norma_14064_1_19

ISO 14064-3:2019

EN 14065:2016

EN ISO 14644-5:2005

EN 14804:2005

UNI CEI EN ISO 14971:2020

UNI EN 15713:2009

EN 16636:2015

ISO 17100:2015

ISO 17100:2015+A1:2017

ISO 18295-1:2017

ISO 20121:2024

ISO 20400:2017

UNI EN ISO 20700:2018

ISO 21001:2018

ISO 21500:2020

ISO 21502:2020

ISO 22005:2007

UNI EN ISO 22301:2019

EN ISO 22716:2007

PAS 24000:2022

ISO/IEC 25001:2014

ISO/IEC 25012:2014

ISO/IEC 25024:2015

ISO 26000:2020

ISO/IEC 27032:2023

*norma_27035-1_23

ISO/IEC 27036-2:2022

ISO/IEC 27036-3:2023

ISO/IEC 27701:2019

EN ISO/IEC 27701:2021

ISO 28000:2022

ISO 28000:2022+A1:2024

ISO/TS 29001:2010

ISO/TS 29001:2010

ISO 29990:2011

UNI ISO 29992:2019

UNI ISO 29993:2019

ISO 30415:2021

ISO 31000:2018

ISO 37001:2025

ISO 37301:2021

ISO/IEC 42001:2023

ISO 45003:2021

ISO/PAS 45005:2020

ISO 55001:2014

EN ISO 56002:2021

(EU) Nr. 715/2013

UNI/PDR 74:2019

ISO/TS 29001:2010

EN 9100:2018

EN 9120:2018

BIM - UNI 11337-7:2018

Amfori BSCI

*norma_cac11969_23

ISO 37001:2016

ISO 10002:2014

ISO 10004:2012

SA8000:2014

ČSN ISO 10006:2019

ISO/TS 29001:2010

ISO/TS 29001:2010

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Suspended and withdrawn certificates

certificate number Issue (date) Validity reason of withdrawing
BCS003 2023-07-13 2026-07-12 Removed
E1372 2023-01-18 2026-01-17 Removed
E1448 2023-03-29 2026-03-28 Removed
E1466 2023-04-10 2026-04-09 Removed
E1675 2023-08-10 2026-08-09 Removed
E1729 2023-10-17 2025-11-09 Removed
E1779 2024-01-29 2027-02-27 Removed
E1787 2024-02-13 2027-02-12 Removed
E1891 2024-05-15 2027-05-14 Removed
E1910 2024-05-30 2027-05-29 Removed
E1982 2024-08-12 2027-08-11 Removed
ESM002 2023-04-12 2026-04-11 Removed
FST005 2023-11-10 2026-11-09 Removed
GHC010 2023-11-28 2026-11-27 Removed
H101 2023-02-20 2026-02-19 Removed
HR017 2023-07-21 2026-07-20 Removed
HR021 2023-09-16 2026-09-15 Removed
O1212 2023-03-29 2026-03-28 Removed
O1401 2023-08-10 2026-08-09 Removed
O1459 2023-10-17 2025-11-09 Removed
O1512 2024-01-29 2027-02-27 Removed
O1521 2024-02-13 2027-02-12 Removed
O1539 2024-03-06 2027-03-05 Removed
O1621 2024-05-14 2027-05-13 Removed
O1622 2024-05-15 2027-05-14 Removed
O1743 2024-08-12 2027-08-11 Removed
PIM003 2023-08-02 2026-04-17 Removed
Q3097 2023-01-23 2026-01-22 Removed
Q3216 2023-03-29 2026-03-28 Removed
Q3221 2023-03-15 2026-03-14 Removed
Q3306 2023-05-12 2026-05-11 Removed
Q3416 2023-07-21 2026-07-20 Removed
Q3454 2023-08-04 2026-08-10 Removed
Q3475 2023-09-13 2026-09-12 Removed
Q3574 2023-11-02 2026-11-01 Removed
Q3578 2023-11-08 2026-11-16 Removed
Q3642 2023-12-14 2026-12-13 Removed
Q3650 2023-12-20 2026-12-19 Removed
Q3670 2023-12-31 2026-12-30 Removed
Q3725 2023-12-14 2026-11-29 Removed
Q3727 2023-11-20 2026-11-19 Removed
Q3761 2023-10-13 2026-10-12 Removed
Q3772 2024-02-13 2027-02-12 Removed
Q3823 2024-03-11 2027-03-10 Removed
Q3836 2024-03-19 2027-03-18 Removed
Q3881 2024-04-03 2027-02-14 Removed
Q3964 2024-05-14 2027-05-13 Removed
Q3999 2024-05-30 2027-05-29 Removed
Q4027 2024-06-13 2027-06-12 Removed
Q4072 2024-07-10 2027-07-09 Removed
SA103 2023-01-31 2026-02-12 Removed
SA143 2023-07-19 2026-07-19 Removed
SA167 2023-12-01 2026-11-30 Removed

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Definition of certification

Certification is an act by which an accredited certification body confirms that the management system of the certified organization complies with the requirements of the relevant normative document.

Proof of conformity is a certificate issued to the organization by the certification body, with a total validity period of three years. Management system certification is not equivalent to accreditation, does not replace product certification, and therefore must not be used under any circumstances as proof of product conformity with requirements.

Accreditation system of the Czech Republic

Accreditation system of the Czech Republic

The Czech accreditation system is part of the European accreditation system created by national accreditation bodies. The European accreditation system is established on basis the requirement of uniform approach to the Testing and Certification. National Accreditation Body of Czech Republic is Czech Accreditation Institute (CAI). CAI is a member of international organizations (EA, ILAC, IAF) and signatory of the multilateral agreements of EA (European level), ILAC and IAF (world level) on mutual recognition of accreditation guarantee the professional performance and approach of CAI. Membership in these international organizations and signing of the multilateral agreements guarantee the professional performance and approach of CAI and credibility the accredited bodies including their outputs. Czech accreditation system is managed via basic documents of CAI (MPA - Methodological Instruction for Accreditation) and International documents EA, ILAC and IAF.

The accreditation system in the Czech Republic is managed by the Czech Accreditation Institute, o.p.s. (hereinafter CAI) as the national accreditation body. The Czech Republic's accreditation system is described in the Methodological Guidelines for Accreditation, which define the basic rules, procedures, and criteria for the accreditation of certification bodies. CAI is a valid member of the international organizations EA, ILAC, and IAF, and is a signatory of the EA MLA for mutual recognition of accreditation results in the fields of testing, calibration, and certification, including EMS.

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Management Systems Certification means increasing the credibility of product suppliers or service providers with clients and state authorities.

The basic certification and surveillance audit procedure

The pre-audit:

  • Verifies the precondition of MS compliance with the requirements of the relevant standards
  • Verifies the readiness of the organization for the certification audit

Certification audit

1. Stage 1 audit

Purpose

  • To become familiarized with the scope of the activities of the company being certified (production or services)
  • To verify the conformity of the documented management system with the requirements of the relevant standards
  • To verify the correctness of the certification scope, applicable exceptions, key processes etc.

The output of the stage 1 audit is:

  • The record from the audit team meeting (indicating any weaknesses)
  • A proposal of the date of the stage 2 audit

    2. Stage 2 audit

    • To verify whether the implemented management system meets the requirements of the relevant standard, the  management system policy and legal and other requirements
    • To verify the level of the management system implementation

    The output of the stage 2 audit is:

    • The record from the final meeting of the audit team (indicating any deficiencies)
    • The recommendation of the audit team that the certificate be issued (or not)
    • The Audit Report

    Classification of deficiencies (valid for all types of audits)

    Minor nonconformity

  •  The audit team records a deviation and the client shall determine a corrective action
  • The audit team will check by the subsequent surveillance audit the removal of this deviation
  • Exposure of a deviation does not affect the positive recommendation to certification
  • Exposure non-systemic non-conformity does not affect the positive recommendation to certification 

    Major nonconformity (non-compliance with any requirement of the relevant standard, non-compliance with legislation))

  • The management system or its substantial part is fundamentally contradicts with the some requirements of relevant standard.

    Surveillance audit / re-certification audit

    Upon completion of the certification processes the lead auditor surveillance audits plan, while respecting the basic rule that the date of the 1st surveillance audit shall not exceed 12 months from the last day of the stage 2 certification audit (initial certification).

     

The recertification audit is always started at least before the expiry of the original certification
if the RCA is completed within 6 months of its initiation, the validity of the subsequent certification is linked to the certification decision
if the RCA is not completed within 6 months, a Level II audit must take place and the validity of the certification cannot be linked to the original certification decision

Follow-up surveillance audits after re-certification are usually carried out within 12 months of the previous audit given in the 3-year audit plan.

        Surveillance / re-certification audit verifies that:

  • Certified system is continuously maintained, monitored and improved
  • There is the compliance of management system with regulatory and legislative requirements (feedback to the client)

       Subsequently this audit confirms the compliance (or non-compliance) with the certification requirements.

 

      The audit team

     The approach focused on a satisfying of the clients needs and their expectation, is the main principle of the audit team, while maintaining the compliance with requirements of the relevant standard for the         management system.

 

Management system certification means increasing the credibility of product suppliers or service providers towards their clients and government authorities.

Basic Certification and Surveillance Procedures