Nt1330 Unit 2 Final Report
Steps for making Quality Manual that suits more better for ISO 17025 Accreditation
ISO 17025 Certification, the general requirements for the competence to carry out tests and calibrations, including sampling. It handles testing and calibration carried out using standard methods, non-standard methods and laboratory-developed methods. It applies to all organizations that tests and calibrations. These include, first, second and third - party laboratories, and laboratories where testing and calibration forms part of inspection and product certification.
When a lab applies to ISO 17025 accreditation, one of the most important documents that serve them in the official quality manual. This is the document that outlines all quality control practices …show more content…
Use the right format. There is no single quality manual format that is strictly required by ISO 17025 standards, but most more or less follow a standard format that divides all procedures into neat categories and explains each one in a straightforward way. The main benefit regarding ISO 17025 Manual is that it is in complete editable MS Word format so anyone may add sections based on their specific industry but, for the most part, following a standard format will help make Organizational quality manual more easier to review.
3. Gather input from staff experienced with ISO 17025. As with everything in lab work, experience, transparency and peer discussion only improves the end product. If one can task a single staff member with assembling all the documentation and writing the manual, the result will be better if they have input from staff members who are experienced with ISO 17025 standards. If necessary, consider bringing in an outside consultant with ISO 17025 experience to review materials as draft them.
4. Double check all documentation. Just because a procedure is in the manual—or perhaps even used on the floor—does not mean that it's reflected in all of policies and protocols. Consider one have a complete quality manual, pull together all supporting documentation and make sure the actual procedures match the quality manual's
ISO 17025 Certification, the general requirements for the competence to carry out tests and calibrations, including sampling. It handles testing and calibration carried out using standard methods, non-standard methods and laboratory-developed methods. It applies to all organizations that tests and calibrations. These include, first, second and third - party laboratories, and laboratories where testing and calibration forms part of inspection and product certification.
When a lab applies to ISO 17025 accreditation, one of the most important documents that serve them in the official quality manual. This is the document that outlines all quality control practices …show more content…
Use the right format. There is no single quality manual format that is strictly required by ISO 17025 standards, but most more or less follow a standard format that divides all procedures into neat categories and explains each one in a straightforward way. The main benefit regarding ISO 17025 Manual is that it is in complete editable MS Word format so anyone may add sections based on their specific industry but, for the most part, following a standard format will help make Organizational quality manual more easier to review.
3. Gather input from staff experienced with ISO 17025. As with everything in lab work, experience, transparency and peer discussion only improves the end product. If one can task a single staff member with assembling all the documentation and writing the manual, the result will be better if they have input from staff members who are experienced with ISO 17025 standards. If necessary, consider bringing in an outside consultant with ISO 17025 experience to review materials as draft them.
4. Double check all documentation. Just because a procedure is in the manual—or perhaps even used on the floor—does not mean that it's reflected in all of policies and protocols. Consider one have a complete quality manual, pull together all supporting documentation and make sure the actual procedures match the quality manual's