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Quality Management Plan

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Guest user Created:   Oct 26, 2020 Last commented:   Oct 27, 2020

Quality Management Plan

Hi, I am revising my Quality Management Plan to include risk. How specific should certain risks be detailed in the QMP?

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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.

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Tracey Evans Oct 27, 2020

As a laboratory, although a formal risk management program is not required, you need to address risks efficiently and rate them in a way so that actions can be justified and appropriate to the level of risk.

For more information regarding actions to address risks and opportunities, see the ISO 17025 toolkit document template: Addressing Risks and Opportunities Procedure at https://advisera.com/17025academy/documentation/addressing-risks-and-opportunities-procedure/

and for more information on the five steps to address risks, see the article Five-step laboratory risk management according to ISO 17025:2017 at https://advisera.com/17025academy/blog/2019/12/05/iso-17025-risk-management-in-five-steps/

For a more detailed explanation, you can watch the free webinar How to manage risks in laboratories according to ISO 17025 at https://advisera.com/17025academy/webinar/iso-17025-risk-management-how-to-manage-it-free-webinar-on-demand/

Also have a look at the following for more information - Expert Community Answers

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