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Writing laboratory document and record control procedure

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Guest user Created:   Apr 12, 2023 Last commented:   Apr 12, 2023

Writing laboratory document and record control procedure

How can I write for our laboratory document and record control procedure?

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ISO 17025 DOCUMENTATION TOOLKIT

Step-by-step implementation for smaller companies.

ISO 17025 DOCUMENTATION TOOLKIT

Step-by-step implementation for smaller companies.

Expert
Tracey Evans Apr 12, 2023

Documents and records need to be designed, authored and controlled to be suitable to hold valuable data and information. When you write the procedure for this activity, understand the requirements in clauses 8.3, 8.4, 7.5 and 7.11 first. Then depending on the platform you will use, for example Microsoft Office (Word and Excel), SharePoint, commercial LIMS or other, document the specific process to be followed in the laboratory.

For more information and the availability of toolkit documents and resources from Advisera, see a similar question and answer at https://community.advisera.com/topic/document-and-record-control-procedure-means-what-are-the-procedure-will-include/

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Apr 12, 2023

Apr 12, 2023

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