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1. I would like to know if all the used samples should be a CRM samples in order to obtain the 17025 accreditation and if we could realise just one repetability reproductibility test on one sample and compare the results with a CRM sample.
Method Validation and measurement uncertainty involves investigating the effect of both systematic and random errors on the accuracy of results. This involves two components -trueness and precision. Both these are qualitative descriptions, where bias is measured to represent trueness; and a measure of spread of results, such as standard deviation to quantify precision. Precision studies include repeatability, intermediate precision and reproducibility. Typically you will use a matrix matched reference material (RM), reference method or reference value to determine any bias; while test samples or spiked sample blanks (matrix matched) are acceptable for the precision studies. Of course RMs could also be used. It is important, either way, to represent the entire working range; menaing that low, medium and high range samples should be included.
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2. we use a Spark Atomic Emission Spectrometry to realise the chemical analysis (zinc and aluminium), there is any criteria in the iso 17025 that obligate us to use an ASTM OR AN iso reference and if yes what should we do if our range of work is out the range mentioned if the standard."
The laboratory need not use a standard method, unless a client or the sector specify you must. As an ISO 17025 accredited laboratory you need to select suitable methods and prove through method validation and quality control; they are adequate for the purpose. The involves showing that the inhouse or non-standard method achieves the performance required- for example limit of detection, accuracy, along with suitable low-enough measurement uncertainty. This is where Proficiency testing or interlaboratory studies can be used to evaluate how the nonstandard method performs compared to laboratories who may be using a standard method.
For more information, see the ISO 17025 toolkit procedure Test and Calibration Method Procedure, at https://advisera.com/17025academy/documentation/test-and-calibration-method-procedure/; along with the two supporting documents Test Method Development, Verification and Validation Register and Test Method Development, Verification and Validation Record.
If you have e.g. hundreds of branch offices, then you should specify only the locations of main offices in your ISMS Scope document, and refer to some other document where you list all the branches - this other document could be your internal or public list of branch offices.
If you go for the certification, you should consult with your certification body on how to document the locations.
Here are some materials that will help you with setting the ISMS scope:
1. What is the ideal KPI's to measure the effectiveness of ISMS in an organization?
ISO 27001 does not prescribe which performance indicators should be adopted by organizations, so there is no such thing as an ideal KPI, and organizations must define them according to their needs and objectives. Some common issues organizations should take into account when defining KPIs are:
As general examples we have:
These articles will provide you a further explanation about performance indicators and security objectives:
2. Can the internal auditor participate in the ISMS activities and take some responsibilities e.g review Policies and standards, develop and create missing documents, be an ISMS Advisor...etc
I'm assuming that by "standards" you mean "procedures".
Considering that, in case you only have one internal auditor, he should not participate in the ISMS activities and take responsibility for its implementation and operation, because this would cause a conflict of interest during the audit (an auditor should not audit his own work). In case you have more than one internal auditor available, they can perform some activities, provided that during the audit they do not audit their own work.
This article will provide you a further explanation about internal audit:
These materials will also help you regarding internal audit:
Considering ISO 27001, I suggest these articles from Advisera:
Considering other sources, I suggest:
These materials can also help you:
Considerando a norma ISO 27001, sugiro consultar os seguintes artigos da Advisera:
Considerando outras fontes, sugiro:
Este material também pode ajudar:
1 - What are the key considerations when implementing an ISMF such as the ISO 27001 in a greenfield site – i.e. an organization where there are nothing in terms of security policy or practice. Would we go through the normal workflow of implementing ISO 27001 or are there deviations?
ISO 27001 was designed to be implemented in organizations of any size and industry, so the general steps are the same, including a greenfield site. In fact, in some cases, the absence of previous security policies or practices is good because it does not bring undesired behavior and minimizes resistance to change.
Broadly speaking, after getting support for your project (through approval of the ISMS project plan) and approval of the Procedure for Document and Record Control, you should consider these steps:
To see how documents compliant with ISO 27001 look like, I suggest you take a look at the free demo of our ISO 27001 Documentation Toolkit at this link: https://advisera.com/27001academy/iso-27001-documentation-toolkit/
This article will provide you a further explanation of ISMS implementation:
2 - Can you suggest any additional resources I could use for greenfield implementation?
These materials will also help you regarding ISO 27001 implementation:
Top management has an invaluable role in communicating internally the importance of the environmental management system (EMS), in promoting and in financing the EMS. ISO 14001:2015, clause 5.1, gives some help in answering to your question:
Please check the following information:
No, GDPR doesn't have a conformity mark as CE.
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