Updated procedures, methods, and supporting documents should be retained and made available to personnel. Furthermore, the laboratory shall use the latest version of methods unless not possible to do so. The laboratory must verify methods before introducing them to make sure they can attain the required performance. Other than having an action plan for method development, the laboratory must validate laboratory-developed methods, standard methods, and non—standard methods used outside their intended scope.
In the case of deviation from methods, the customer must document, technically justify, authorize, and accept it. As a general rule, the laboratory must preserve records of validation. The laboratory shall have a sampling method and sampling plan when it executes sampling of products, materials, or substances, for subsequent calibration or testing.
To ensure the legitimacy of subsequent calibration or testing, the sampling method shall address the aspects to be controlled. Just like the other parts, the laboratory must retain records. The laboratory shall have a procedure for the handling, receipt, retention, storage, protection, transportation, disposal, and return of calibration items or tests, including all provisions necessary to protect the integrity of the calibration item or test and to protect the interests of the customer and the laboratory.
Similarly, there should be precautions to avoid contamination, deterioration, loss, and damage to the item during handling, storing, waiting, transporting, and preparing for calibration or testing.
Handling instructions provided with the item shall be followed. The laboratory must have a system for the unambiguous identification of calibration items or tests. The laboratory must maintain records of the calibrated item or tests. This is about adequate information and tracking amendment to original observations or previous versions. To further explain, the laboratory shall assure that technical records for laboratory activities include sufficient results and reports. It must cover information to facilitate and identify factors affecting the measurement result and its associated measurement uncertainty, and enable the repetition of the laboratory activity under conditions as close as possible to the original.
The technical records shall enclose the date and the identity of personnel responsible for each activity such as checking data and results. Laboratories shall identify the contributions to measurement uncertainty. All significant contributions, including those coming from sampling, shall be included using appropriate methods of analysis when evaluating measurement uncertainty.
The laboratory shall be responsible for having a procedure in monitoring the validity of results. It includes checking the performance by comparison with the results of other laboratories.
Finally, it must take action when data from the monitoring are found to be outside of pre-defined criteria. A laboratory meets at least the intent of the management system requirements specified in 8.
If for whatever reason during the FIRST 90 days of your purchase, you are not satisfied for any reason, simply contact support qse-academy. You can customize them by adding company logos and colors, and edit headers and footers to match your favorite style. To complete them you must fill in only the name of the company, the responsible parties, and any other information unique to your company.
We presented the ISO documentation, so as to assure all its users that they have completed everything accurately and with the utmost efficiency. All the documents are made so that you can follow the proposed order perfectly, which allows you to make sure that nothing is missing, and that no one gets lost in the process.
The included comments and flowcharts help your staff understand each document and its usefulness, which helps you to make quality management more fluid, and processes easier to follow. Yes, all the documents required by ISO are included, as well as the quality policy and the current but optional procedures. Instant Delivery — The package is downloadable immediately after purchase Free Consultation — In addition, you can submit two complete documents for review by professionals. Created for your business — The models are optimized for small and medium businesses.
We also got so much information from our email and one-on-one sessions, which led to our employees becoming fully informed about how to comply with the requirements. He recalled how QSE Academy toolkits made their implementation simple and productive. Indeed, consultants from QSE Academy were very hands-on even if the documents they have provided are well-explained and very detailed. Your download should start in a few seconds.
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Here are the instructions how to enable JavaScript in your web browser. This procedure covers all tests and calibrations carried out in the laboratory. Can I edit the document? The document is fully editable — just enter information specific to your company. Can I use this to become accredited? The documentation template may be used for ISO accreditation audit purposes.
Well-defined instructions Document templates contain an average of twenty comments each, and offer clear guidance for filling them out.
Designed with your company in mind The template was created for small and medium-sized businesses. Documents include placeholder marks for all information you need to complete.
Each document includes comments and information , which guides you through completion. View full-size preview. Buy Test and Calibration Method Procedure.
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