Steps for Making Quality Manual that Required 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 define structure complete QMS is known as the quality manual. This is the document that outlines all quality control practices and supporting procedures in place. Making this manual is a daunting task, but if done right, will simply make it your accreditation process. So what makes a quality good enough for ISO 17025 accreditation? Here are four of the pillars:

Make sure your practices are in order: A common problem with labs prepare resembles their first ISO 17025 accreditation processes is that they also focused on the accreditation itself rather than on the internal practices that the accreditation is based on become. This can lead to the creation of an ISO 17025 Quality Manual which looks much better than practicing self-but each ISO 17025 accreditation auditor goes to the different brands quickly. Thus, the best way to approach creating quality manual is an opportunity to review and improve its internal processes. In this way, this quality manual is much more than an item on a checklist - it is a leading force for improvement within the organization, which is exactly what it is intended.

Use the right format: There is no single quality manual format is strictly required by the ISO 17025 standards, but most are more or less follow a standard format that all procedures in neat categories distributes and puts each in a simple way. The main advantage with respect to ISO 17025 Manual is fully editable MS Word format so that everyone shares to add based on their specific sector, but for the most part, will assist in response to a standard format for Organizational Quality Manual easier revised.

Gather input from staff experienced with ISO 17025: As with all work in the lab, experience, transparency and peer discussion only improves the end product. If one single member of staff with the merging of all documentation and writing the manual task, the result will be better if they have input from people who have experience with the ISO 17025 standards. If necessary, consider using an outside consultant ISO 17025 experience to review materials as draft them.

Double check all documentation: Just because a procedure is in manual or maybe even used on the floor does not mean it will be reflected in all policies and protocols. Consider a have a complete quality manual, pulling together all supporting documentation and make sure that the actual procedures match the quality of the progress of the manual.