ISO 17025 is the general requirements for the competence of testing and calibration laboratories and is the main Standard of ISO used by testing and calibration laboratories. Main objective of the ISO 17025 Certification in Singapore is to ensure the technical competence and reliability of analytical results. It is used in management requirements and technical requirements that influence the improvement of the quality of the work carried out in the laboratories.
ISO 17025 is useful to any business company that performs testing sampling and reliable results. This includes all types of owned laboratories business and operated by the Government, industry, or any type of organization. The ISO 17025 standard is also useful for Universities, research centers, inspection bodies, product certification organizations, and other conformity assessment bodies, with the need to do testing sampling.
How to get ISO 17025 Accreditation:
The Process of accreditation involves multiple steps including document review, process audit, and accreditation results that are provided by third party accreditation.
1.Start your Preparation:
First you start your research and learn about the 17025. Take the training about ISO 17025 and discover what the individual requirements are. Learn the scope of accreditation and different requirements, including general, structural, resource and process requirements, to prepare yourself at all stages of organizations.
2.17025 Gap analysis and checklist:
Improvement in your laboratory management system to meet the management and technical requirements of an ISO 17025 Registration in Australia Gap analysis helps you identify what your lab already has and how much time you take to complete the accreditation process.
3.Creat your 17025 implementation plan:
Prepare a framework for approaching accreditation bodies by referring to the checklist created in the earlier level. Plan a workflow and timeline of the level that you will follow while applying for accreditation and beyond.
4.Documentation:
In this stage you will need to document all the processes, methods and procedures of the lab. Proper documents are included.
5.Audit QMS performance:
For this yor lab needs to conduct the audits to learn about any non conformities based on the internal audit and action plan. This will suggest your lab in correcting any issues before beginning the accreditation assessments.
6.Final audit for an accreditation body:
The final assessment of the lab will be performed by an accreditation body. They may
Interview some of the workers of your lab. Inspect the documents and records, observe the selected test and examine the equipment. They look for statements, documented procedures, records, and policies to check your lab’s technical competency.
Our advice:
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