ISO 17025 Certification
in Riyadh

ISO 17025 in Riyadh

ISO 17025 Testing and Calibration in Riyadh:
ISO 17025 is the international standard  for the requirements for organizations   that perform testing, sampling  and calibration services.   The requirements address their ability to provide  valid and reliable results from those services.
ISO/IEC 17025:2017 TESTING AND CALIBRATION LABORATORIES
ISO/IEC 17025 is the international standard that sets forth the general requirements for the competent, impartial, and consistent operation of laboratories. It outlines the activities necessary for laboratory operation to instill confidence in its ability to produce valid and consistently reliable testing, calibration, and sampling results. The most notable changes between the 1999 and 2005 releases include a significant emphasis on the responsibilities of senior management, requirements for continual improvement of the management system itself, and improved communication with customers. The 2005 version of the standard condenses into five elements: normative references, terms and definitions, management requirements, and technical requirements. Management requirements primarily pertain to the operation and effectiveness of the laboratory’s quality management system, while technical requirements encompass factors essential for the accuracy and reliability of tests and calibrations conducted in the laboratory. The 2017 version of ISO/IEC 17025 has restructured this framework to include scope, normative references, terms, and definitions.
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    Requirements of ISO 17025 in Riyadh

    General requirements, structure requirements, resource requirements, process requirements, and management system requirements are integral components of ISO/IEC 17025-2017, the current revised standard for laboratory accreditation. General and structure requirements pertain to the organization of the laboratory itself, while resource requirements address issues related to personnel, facilities, and other resources utilized by the laboratory to produce technically valid results. Process requirements form the core of the standard, delineating activities to ensure results are grounded in accepted scientific principles and maintain technical validity. Management system requirements encompass steps taken by the organization to equip itself with quality management system tools that support the production of technically valid results.

    ISO/IEC 17025-2017 was developed through collaboration between the International Organization for Standardization and the International Electrotechnical Commission. Unlike certification according to ISO 9001 or ISO 14001, which signifies the presence of an effective management system, ISO/IEC 17025 accreditation recognizes the technical competence of laboratories. Accreditation involves formal delegation by the accreditation body following assessment and confirmation that the laboratory effectively meets the requirements of ISO 17025 to perform tests within its accredited scope.

    This standard and accreditation are utilized by independently owned and operated laboratories, as well as those within large organizations, across various industries and sizes engaged in sampling or measurement activities. This includes regulated government and public sectors, as well as non-regulated sectors.

    Together with ISO 9001, ISO/IEC 17025 forms the basis for ISO 15189, which outlines specific requirements for competence, quality, and accreditation of medical laboratories.

    What are the testing and calibration laboratories?

    Testing laboratories analyze the characteristics of items of interest for conformity assessment. For instance, they may test a sample to determine if its pressure levels comply with legislated limits. Calibration laboratories, on the other hand, compare the accuracy of a measurement instrument of unknown accuracy to one with known accuracy. For example, calibration ensures that the airport scale accurately weighs luggage by comparing its readings against certified mass pieces. 

    ISO/IEC 17025 plays a crucial role in laboratory sampling, testing, and conformity assessment, which are essential for technological advancements and quality assurance. It harmonizes procedures and standard methods, facilitates collaboration among laboratories and other stakeholders, and promotes the acceptance of results across countries.

    Why is ISO or IEC 17025:2017 accreditation a good idea for your Organization?

    1. The benefits range from strategic enhancements to external business advantages to internal improvements. A few are highlighted here, including increased customer confidence.
    2. Accreditation to ISO/IEC 17025:2017 demonstrates that a laboratory is capable of consistently providing valid results, that individuals performing the work are competent, and that all accredited measurement results can be traced back to the International System of Units or appropriate references. This primary objective is crucial for customers to ensure that results are accepted internationally.
    3. Establishing a proactive, risk-based business and quality culture, as opposed to a reactive one, defines activities, policies, and quality objectives that form the foundation for the organizational strategy direction. A current of risk-based thinking drives cost-effective operations and evidence-based decision-making. Laboratories must plan actions to address risks, drive improvements, and ensure that major quality risks related to testing and calibration are identified, controlled, and consistently carried out. Acquiring accreditation from a third-party body verifies that tests and calibrations are performed correctly by trained laboratory professionals.
    4. Fostering an environment of professionalism and pride involves undergoing third-party assessments, where auditors scrutinize all aspects of your work. Although challenging, once the audit is over, there is a sense of accomplishment and pride. Third-party accreditation instills a sense of pride throughout the entire organization.

    What are the steps to become ISO or IEC 17025 accredited in Riyadh?

    To achieve accreditation, start by obtaining a copy of ISO/IEC 17025:2017 and familiarizing yourself with its requirements. Contact an ISO 17025 accreditation body and understand their criteria. Plan training sessions for all personnel, especially those involved in management, technical activities, and internal auditing.

    Define and document the laboratory activities for which you seek accreditation, along with the quality objectives. This provides context for determining the extent to which risks should be controlled and processes documented. Conduct a gap analysis to identify discrepancies between current practices and the standard’s requirements.

    While a manual may not be required, it’s beneficial for documenting laboratory policies and objectives. Develop necessary procedures and ensure records are linked, kept, and maintained. Before applying for accreditation, ensure all mandatory processes are documented, and records demonstrate implementation.

    Establish an ongoing internal audit program and maintain records of management reviews and methods validation. Following a remote review of documentation and activities, the accreditation body will approve recommendations and schedule the accreditation audit. Prepare about six months’ worth of activities and objective evidence for review before accreditation recommendation.

    Benefits of ISO 17025 in Riyadh

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    FAQ

    The ISO 27001 certification of an organization demonstrates its commitment to information security excellence, which lowers risks, complies with legal requirements, and cultivates stakeholder trust.

    The timeline for ISO 17025 Certification varies depending on the organization’s size and complexity but typically ranges from 3 to 12 months.

    ISO 17025 Certification enhances credibility, facilitates global recognition, improves operational efficiency, boosts customer satisfaction, and provides a competitive advantage.

    Our ISO 17025 Certification cost is competitive and transparent, with no hidden charges. We provide a detailed cost estimate upfront.

    While it’s possible to achieve ISO 17025 Certification without a consultant, hiring an experienced consultant can streamline the process, ensure compliance, and save time and resources.

    Contact us today for a free consultation and take the first step towards ISO 17025 Certification with confidence.

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