How to consistently implement ISO requirements?

I assume you are referring to the general requirement (clause 8.1.1) to demonstrate the consistent achievement of the requirements of ISO 17025. Once implementation is complete, meaning all the processes and required documentation have been put in place; the objective is the consistent operation of the laboratory to support the policies, achieve the quality objectives and drive improvement in the performance of the laboratory management system.

This is achieved by having processes and procedures, for example handling nonconforming work and corrective actions, that are firstly effective in meeting each ISO 17025 requirements, meaning implemented and achieves what was intended. Secondly you should aim for efficiency where the activity is performed in the best possible way with the least waste of time and other resources). Monitoring, evaluation and assessment activities such as quality control, ongoing competency evaluation of personnel, auditing and management reviews are used to provide information to be acted on to ensure continuing adequacy of the management system. Data, information and records such be kept to provide objective evidence of this consistent achievement.

For more information to meet ISO 17025 requirements, see the complimentary white paper (PDF) Clause-by-clause explanation of ISO 17025:2017 available at https://info.advisera.com/17025academy/free-download/clause-by-clause-explanation-of-iso-17025/ and the ISO 17025 Toolkit at https://advisera.com/17025academy/iso-17025-documentation-toolkit/