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Testing laboratory · Resolution No. 323 · O‘z DSt 3410:2019 · Uzbekistan
Approval of a testing laboratory in Uzbekistan: preparation under Resolution No. 323 and O‘z DSt 3410:2019
We connect the approval scope, test methods, equipment, personnel and technical records into one working system and prepare the laboratory for assessment by the authorized body.
Standart Consult performs preliminary diagnostics, builds a realistic scope, checks the methodological and technical base, develops documents and helps resolve findings. You receive not a folder of generic templates, but a system that matches the actual work of your laboratory.
Working under the current Resolution No. 323
Prepared for the actual work of the laboratory
Linking methods with equipment
Preparing personnel and records
Supporting corrective actions
Comprehensive preparation
Preparing the laboratory for real assessment, not just a document package
The main reason for findings is a gap between the declared scope, the documents and how the laboratory actually performs testing. We close this gap before submission and assessment.
- we diagnose the laboratory’s current readiness;
- we define a justified approval scope and applicable methods;
- we compare methods, ranges, equipment and measuring instruments;
- we prepare procedure documents, a technical passport, journals and record forms;
- we prepare personnel for practical questions and support corrective actions.
Result for the customer
A laboratory able to demonstrate competence in practice
ScopeScope items are supported by methods, personnel and the technical base.
DocumentsProcedures and forms reflect the laboratory’s actual processes.
EquipmentInstruments and records are linked to the declared tests.
PersonnelEmployees understand the methods, records and their responsibilities.
Who this service is for
Preparation tailored to the condition and objectives of your laboratory
New testing laboratory
We define the scope, methods, equipment, premises and documents before the application is submitted.
Production laboratory
We turn internal control of products, raw materials and materials into a system supported by records.
Operating laboratory
We review existing documents, methods and equipment and remove inconsistencies between them.
Scope extension
We assess which new parameters and methods can be justifiably added to the approval scope.
After receiving findings
We review the assessment report, prepare corrective actions, updated documents and supporting records.
Before purchasing equipment
We help define the technical need in advance to reduce the risk of unnecessary or unsuitable purchases.
What is included
The complete preparation chain for a testing laboratory
1
Diagnostics and approval scope
- analysis of the tests actually performed;
- review of products, parameters, ranges and methods;
- development of a realistic scope without unsupported items.
2
Methods and technical base
- review of the current validity of regulatory documents;
- matching methods with equipment and measuring instruments;
- analysis of premises, conditions and reference materials.
3
Documents and technical records
- procedure documents and the technical passport;
- journals, worksheets and test report forms;
- documents on personnel, equipment, samples and nonconformities.
4
Implementation and support
- training employees to work with documents and records;
- checking practical readiness for the commission’s questions;
- assistance with submission and resolution of findings.
The key linkage
How we connect the scope, methods and evidence of competence
| Scope element | What is checked | Methodological basis | Equipment and records |
|---|---|---|---|
| Product or test object | Whether the product, material, sample or process is defined correctly. | Technical regulations, O‘z DSt, GOST, ISO, IEC and applicable procedures. | Sample identification, storage conditions, journals and reports. |
| Parameter or characteristic | Whether the parameter is supported by personnel competence and the capabilities of the method. | Method standards, instructions and documents confirming method applicability. | Working records, calculations, condition monitoring and responsible personnel. |
| Method and range | Whether there is a clear procedure, range and criteria for the result. | Current regulatory and methodological documentation. | Test equipment, measuring instruments, verification or calibration, and maintenance. |
| Test conditions | Whether factors affecting the reliability of the result are controlled. | Method requirements and the laboratory’s internal procedures. | Monitoring instruments, condition logs and records of nonconformities. |
Typical risks
Why laboratories receive findings
The commission assesses not the appearance of the documents, but the laboratory’s ability to perform the declared tests. Generic templates therefore do not protect against findings when they do not match actual operations.
- the scope includes tests without suitable equipment;
- the procedure is not linked to worksheets and the report;
- there are no records of condition, verification, calibration or maintenance;
- personnel cannot explain how the method is performed;
- conditions affecting the result are not controlled;
- corrective actions are documented without evidence that the cause was removed.
Why templates are not enough
The commission assesses your laboratory, not an example from a ready-made package
Documents must match specific methods, equipment, structure, personnel and technical records. We adapt the system to actual operations and verify its use before assessment.
Check the possible risks for your laboratory →New laboratory
We first define the scope and technical need, then build the document package.
Operating laboratory
We identify gaps between methods, instruments, report forms and actual records.
After assessment
We review findings and prepare corrective actions with supporting evidence.
How we work
How preparation with Standart Consult is organized
1
Initial assessment
We clarify the testing direction, document status, equipment and the laboratory’s objective.
2
Preparation plan
We prepare a list of tasks, missing documents and technical issues.
3
Development and implementation
We prepare documents, records and the scope, train employees and check implementation.
4
Support
We assist with submission, preparation for assessment and resolution of identified findings.
Submission support
We help prepare documents and support submission of the application for laboratory approval
The application is submitted on behalf of the applicant through a Public Services Center, the Single Portal of Interactive Public Services or the national “Technical Regulation” information system. The main challenge is not the submission itself, but the correct preparation of the scope, list of methods, procedure documents, technical passport and supporting materials.
Standart Consult checks completeness, helps complete the application and prepare attachments, prepares the laboratory for assessment and organizes work to resolve findings. Access to the personal account and the electronic signature remain with the customer — we support the process without replacing the applicant.
What we check before submission
- justification of the approval scope;
- list of methods and types of measurement;
- laboratory procedure documents;
- technical passport and equipment information;
- record forms and personnel readiness.
Regulatory basis
Current documents for approval of testing laboratories
Resolution No. 323 dated 24 June 2026
Approves the Administrative Regulation for the public service of approving the technical competence of testing laboratories. Effective from 25 June 2026.
O‘z DSt 3410:2019
The state standard “General requirements for the technical competence of testing laboratories”. Applicability of the requirements is assessed together with documents for specific test methods.
Important: Resolution No. 456 dated 28 July 2020 ceased to be effective on 25 June 2026. Materials referring only to the former procedure must be updated. Official text of Resolution No. 323 on Lex.uz.
Laboratory approval
A national procedure confirming technical competence in the declared scope under Resolution No. 323 and applicable technical requirements.
Accreditation
Confirmation of competence within the accreditation system, generally against ISO/IEC 17025, with official accredited status.
Electrical Testing Laboratory Approval
A dedicated route for electrical testing laboratories with specific requirements for testing, safety, personnel and equipment.
Practical specialization
Why Standart Consult is suitable for preparing testing laboratories
A team specializing in laboratories and technical competence
We work at the intersection of regulatory requirements and actual laboratory operations. We therefore treat scope, methods, equipment, personnel and records as one system rather than separate templates.
- preparation of testing and electrical testing laboratories;
- accreditation, approval, ISO/IEC 17025 and O‘z DSt 3410:2019;
- development of test and measurement procedures, journals, reports and technical records;
- analysis of equipment and its conformity with declared methods;
- preparation of corrective actions for findings.
FAQ
Frequently asked questions about testing laboratory approval
Approval confirms the technical competence of a testing laboratory in the declared scope. The relationship between the scope, methods, equipment, personnel, premises, documents and technical records is assessed.
The current procedure is established by Resolution No. 323 dated 24 June 2026, which approved the Administrative Regulation for the public service. The former Resolution No. 456 ceased to be effective on 25 June 2026.
O‘z DSt 3410:2019 contains general requirements for the technical competence of testing laboratories. Resolution No. 323 establishes the public service procedure, while the standard and method documents are used to assess technical readiness.
Approval confirms technical competence under a national procedure. Accreditation is carried out within the accreditation system, generally against ISO/IEC 17025, and is linked to official accredited status.
It is possible to prepare documents independently. However, findings are often caused not by missing text, but by a gap between the scope, documents and real work. Independent diagnostics help identify such inconsistencies before assessment.
Templates describe an imaginary laboratory, while your laboratory is assessed. Documents must match actual methods, equipment, personnel and records; otherwise, they may themselves become a source of findings.
Yes. It is useful to define the scope and methods first, and then the technical need. This reduces the risk of buying instruments that do not cover the declared tests or turn out to be unnecessary.
Yes. Work begins with diagnostics of the actual tests, methods, equipment, personnel and premises, after which the document and record package is built from scratch.
Each nonconformity must be reviewed, its cause determined, corrective actions prepared, documents updated and evidence of actual resolution collected. We help organize this work.
They depend on the breadth of the scope, the current condition of documents, availability of methods and equipment, personnel readiness and whether the system must be built from scratch or only refined. The estimate is prepared after the initial diagnostics.
The official decision is made by the authorized body. Standart Consult prepares the laboratory, scope, documents, personnel and evidence of competence, but does not replace the official assessment and cannot guarantee the decision of a public authority.
Initial assessment
Get a preliminary assessment
Not sure whether the laboratory is ready for approval?
Submit a request. We will clarify the proposed scope, document status, methods and available equipment and advise which stage to start with.
1
We will contact you
We will clarify the direction and current situation.
2
We will ask a few questions
About the scope, methods, equipment and documents.
3
We will propose a format of work
Preparation from scratch, refinement, extension or resolution of findings.
Preliminary assessment of laboratory readiness
Tell us about your laboratory — we will advise where to start
After your request, we will contact you, clarify the scope, document and equipment status, and suggest a suitable preparation format. The official approval decision is made by the authorized body.
