Importance of ISO 17025 in Testing For the first time, emphasizing the analysis of risk and increasing attention to the staff's professional skills employed in testing/calibration activities to guarantee transparency and impartiality for the customer. Accreditation lasts three years, during which the laboratory will be subjected to periodic annual checks. The number of tests to be accredited requested in the first instance can increase by requesting an extension from Accredia during the periodic reviews. The points of the standard can be divided into the following macro-categories:
Resource Requirements: In this chapter, you need to define the competency requirements of the staff.
Structural requirements: to comply with the provisions of this chapter, the laboratory must identify the management that has overall responsibility for the laboratory; define and document the test, calibration, or sampling activities that you want to accredit, and declare compliance with the ISO 17025 standard. General Requirements: this chapter describes the requirements that the laboratory adopts to ensure impartiality and confidentiality Process Requirements: for this chapter, the laboratory must equip itself with procedures for reviewing requests, offers, and contracts; method selection, verification, and validation; sampling; handling of the objects.
Management System Requirements: the laboratory for this chapter can choose two options: list the minimum requirements for implementing a management system in the laboratory or have a management system compliant with the needs of the ISO 17025 Templates standard.
ISO 17025 consultancy, acts as a guide and as an effective support to all laboratories that have to confront and adapt to the requirements of UNI CEI EN ISO 17025: 2018. ISO 17025 Accreditation will take care of the following activities: An initial check-up to identify the context in which the laboratory operates, the type and number of tests subject to accreditation. Drafting and implementation of the laboratory quality management system consisting of the following documents: manual, management, and operational procedures governing the laboratory processes. Support for new risk management in the laboratory. Internal audit on the state of compliance achieved with the drafting of an audit report on the findings. Support for the drafting of the Management Review Support during audits Their goal is to offer private and public companies innovative services and solutions and customized intervention plans, guaranteeing consultancy "tailored" to the client. The advantages According to the ISO 17025 standard, implementing a management system allows Laboratories to offer a "guarantee" service compared to non-accredited Laboratories: as the Certificates of Analysis issued for accredited tests are "legal." Therefore, the laboratories become a reference point for safety and guarantee for both client companies and control bodies. Thus, obtaining and maintaining ISO / IEC 17025 accreditation with help of ISO 17025 Consultant entails the following advantages: Access to public and private calls for tenders aimed exclusively at ISO / IEC 17025 accredited laboratories. Possibility to communicate to the outside the obtainment of the ISO / IEC 17025 accreditation. Improvement of the image of the laboratory on its technical competence (relating to accredited tests/calibrations). Acquisition of new customers who require accreditation according to ISO / IEC 17025 for the conduct of tests/calibrations. Obtaining an internationally recognized accreditation. This type of certification plays a fundamental role in meeting the requirements of legislation minimizing the risks of the products connected to their placing on the market, and developing a safe product capable of being marketed worldwide. Conclusion: Cal Lab Access provide assistance for the preparation and forwarding of the documentation to ACCREDIA preparatory to the start of the accreditation process.
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