- Views: 8
- Report Article
- Articles
- Business & Careers
- Business Ideas
Iso Certification In Kuwait
Posted: Dec 21, 2019
ISO Certification in Kuwait plays a prominent role in laboratories of every organizations. ISO 17025 standard focus on providing the valid results and testing calibration in the laboratories in the organizations.
Technical requirements address the competence of staff; testing methodology; equipment and quality; and reporting of test and calibration results. Implementing ISO/IEC 17025 has benefits for laboratories, but the work and costs involved should be considered before proceeding.
What is ISO 17025?
ISO/IEC 17025 is the global quality standard for testing and calibration laboratories. It is the basis for accreditation from an accreditation body. The current release was published in 2005. There are two main clauses in ISO/IEC 17025 – Management Requirements and Technical Requirements. Management requirements are related to the operation and effectiveness of the quality management system within the laboratory, and this clause has similar requirements to ISO 9001.
The ISO 17025 standard (General Requirements for the Competence of Testing and Calibration Laboratories) by members of the International Standards Organization in December 1999 (ISO 17025:1999, 1st Ed., 1999, ISO, Geneva, Switzerland, pp 12–15), Factocert helps further developed its quality system by adding components to achieve accreditation to ISO 17025. The additional components of the new standard specifically dealt with technical requirements for processes and analytical methods. Factocert helps the laboratories became accredited in March 2001. Factocert helps the laboratories implemented ISO 9002 first because the ISO 17025 standard was not available. Currently, laboratories accredited to ISO 17025 maintain quality system parameters in line with ISO 9002. Maintaining dual accreditation or certification is not required, but may be beneficial. The benefits include more frequent audits by external auditors to keep the system sharp and the emphasis on customer requirements and satisfaction driven by the ISO 9000 standard series.
Implementing ISO/IEC 17025 as part of laboratory quality initiatives provides both laboratory and business benefits such as:
Having access to more contracts for testing and/or calibration. Some public and private organizations only give contracts to accredited laboratories. Accreditation will also help to get more contracts from organizations that don’t mandate accreditation, but do give preference to accredited laboratories in competitive situations.
Improved national and global reputation and image of the laboratory.
Continually improving data quality and laboratory effectiveness.
Having a basis for most other quality systems related to laboratories, such as Good Manufacturing Practices and Good Laboratory Practices. Analytical testing laboratories seeking ISO/IEC 17025 will be impacted in multiple areas. The main difference between good analytical practices and formal accreditation is the amount of documentation to be developed. There is no doubt that any good analytical laboratory uses qualified analysts, checks the performance of equipment used for testing, and validates analytical methods. However, many times the outcome of the tests is not fully documented. ISO/IEC 17025 accreditation requires formal documentation for nearly everything.
ISO 17025 Specific requirements include:
Sampling should be performed according to a sampling plan, and all sample details should be documented. Samples should be uniquely identified and the sample integrity should be protected during transport and storage. The quality of test results should be monitored. Test reports should include test results as well as an estimation of the overall measurement uncertainty. The report should also include either detailed information about the sample and test conditions, or a link to a reference document.
Records should be properly maintained to ensure data integrity and availability. Some requirements impact more than one workflow step: All analytical methods and procedures should be validated. This includes methods and procedures for sampling, testing and data evaluation.
Equipment used for sampling and testing should be calibrated, tested, and well maintained. Material such as calibration standards should be qualified and traceable to System International (SI) units or to certified reference material.
Why Factocert is the best consultation company!
Our Consulting methodology are established by expert Consultants with their domain experience following many years in order to fulfil the customer requirements enabling Factocert to be the topmost solution in the industries. Client Count on Factocert to assist the transformation with respect to development of Management in a best way possible. Our vision is to beat a winning Culture by living are values organisation and creating a progressive environment in the industry to lead a well-structured developed organisation. The customers, Factocert is having will always be the very most important relationship for us to handle.
We aim to be the most competitive and productive service providing organisation. The competency in the Marketplace is having a tough competition from Factocert.
About the Author
Factocert is an Epitome of consultation inculcating industry best practices. Our pragmatic approach delineates the requirements of ISO Standards, CE Mark, VAPT, Six Sigma, Process Audit and other International Standards.
Rate this Article
Leave a Comment