Check a CIM/ICM contribution about that! http://www.cim2017.com/

Ok sir .Means need to buy first ....

Try to read
https://www.eurachem.org/index.php/news/newsarts/230-nws-iso17025-2017

Contribution of CIM 2017 should give you all information that you need.

Also take a look at the official ISO summary document at https://www.iso.org/publication/PUB100424.html .

No I mean that is possible to read without payment

Thanks all for your cooperation .It's great help for me .

I have not read the latest version of ISO 17025:2017 However among and during the discussions i came to understand that in the latest version the management requirements are aligned with quality management requirements of iso 9001 2016 where in much emphasis is given on risk assrssment rather than root cause analysis and preventive measures. technical requirements being almost the same
however one has to read thoroughly the new standard along with the iso 9001.

There are no big changes
You can continue using your current quality manual or you can identify your activities and responsibilities
The term of quality manager and technical manager no more existing i.e you identify the activities and who responsible to perform them(but you can leave it as quality manager and Technical manager)
Quality policy sholud be modified to include impartiality
Imapartiality should be identified and it is impacts and how to avoid them
Risk managements should be identified

Mahmoud voila une tres bonne synthésse. Very nice synthesis.

Is there any strategy for risk Assessments as for ISO/IEC 17025.

Risk assessment are cloe to the current 4.9 and preventive action. Risk on the testing process

Here in both reference languages
https://www.scc.ca/fr/nouvelles-et-activites/nouvelles/2017/revision-de-iso-iec-17025
https://www.scc.ca/en/news-events/news/2017/changes-iso-iec-17025