Welcome to Laboratory Management System Consultancy Portal

About LMS & benefits of consultancy

Consultancy solutions to implement laboratory management system for resilient & smarter businesses

Description 

IEC stands for International Electrotechnical Commission which in collaboration with ISO creates the specific system for global standardization. ISO/IEC 17025 is used for testing and calibration laboratories and recognized globally. It was established with the purpose of offering quality and improving the processes within laboratories. It has two main clauses; Management Requirements which are related to the performance and efficiency of the Quality Management System inside the laboratory, and Technical Requirements which focus on the capabilities of employees, testing methodology, equipment, and the test and calibration results.

Course details
Benefits of ISO/IEC 17025 Laboratory Management System:
1- Gain the competitive advantage
2- Growth of laboratory effectiveness
3- Improved access to more contracts for testing and calibration
4- Offer expertise on improving work processes
5- Offer more reliable and efficient lab testing and results
Technical information
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
4.1 Impartiality
4.2 Confidentiality
5 Structural requirements
6 Resource requirements
6.1 General
6.2 Personnel
6.3 Facilities and environmental conditions
6.4 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 Handling of test or calibration items
7.5 Technical records
7.6 Evaluation of measurement uncertainty
7.7 Ensuring the validity of results
7.8 Reporting of results
7.9 Complaints
7.10 Nonconforming work
7.11 Control of data and 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)
8.5 Actions to address risks and opportunities (Option A)
8.6 Improvement (Option A)
8.7 Corrective actions (Option A)
8.8 Internal audits (Option A)
8.9 Management reviews (Option A)
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