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You can use ISO 20000 as a management system (or a framework) towards excellence in service delivery. However, use ITIL as well, to manage daily activities and as an improvement model.
ITIL4 guidelines can help you evolve your organization in a way to converge technology and business.
Here is an introduction article in ITIL4 "ITIL 3 vs. ITIL 4 – What has changed and what is new?“ https://advisera.com/20000academy/blog/2019/07/04/itil-3-vs-itil-4-what-has-changed-and-what-is-new/
According to ISO 20000, SLA is "documented agreement between the organization and the customer that identifies services and their agreed performance."
Here are a few articles where you can find more details:
"What’s the content of an ITIL/ISO 20000 SLA?" https://advisera.com/20000academy/blog/2016/06/14/whats-the-content-of-an-itiliso-20000-sla/
"SLAs, OLAs and UCs in ITIL and ISO 20000" https://advisera.com/20000academy/knowledgebase/slas-olas-ucs-itil-iso-20000/
I will not comment your auditor’s comment about doing the follow-up.
Please consider this flowchart:
When you receive the audit report a first step is to separate minor from major nonconformities.
About the minor nonconformities
The auditor found one nonconformity. As a good practice your organization should check if there are other situations not audited with the same nonconformity. A minor nonconformity requires a correction. An action to eliminate the nonconformity. Define the correction, implement that correction and shortly after check that the nonconformity was removed. For example, the auditor found an outdated form at the warehouse. Your organization check all forms in use and finds another outdated form at the sales department. Remove outdated forms and distribute the updated ones. One-week later check that the right forms are being used at the warehouse and the sales department. All these steps should be recorded in a form for treating audit minor nonconformities.
About the major nonconformities
The auditor found one nonconformity. As a good practice your organization should check if there are other situations not audited with the same nonconformity. A major nonconformity requires both a correction to eliminate the nonconformity and a corrective action to eliminate the cause of the nonconformity. Define the correction, implement that correction and shortly after check that the nonconformity was removed. At the same time, investigate what are the possible causes of the major nonconformity and determine the root cause(s) of that major nonconformity. Then determine a corrective action to eliminate that/those root cause(s). Implement that corrective action and shortly after check that the corrective action was implemented. After some agreed time, check that the implemented corrective action was effective. For example, an organization took to much time to answer to complaints. Their internal procedure mentioned less than 24 hours for a first answer while they had on average more that 60 hours. 3 months after implementing the corrective action they concluded that the average time for the first answer was 12 hours. The corrective action was effective.
Please ensure that implementation and effectiveness is verified by someone not working on the department or area where the nonconformity took place.
You can find more information below:
What do you mean by archived documents?
If you mean records – the answer is yes. Records are the memory of an organization. If an organization lose or cannot access the records in time, it has no memory. An organization without memory is an organization that learns slowly. An organization must define rules to archive records in order to be clear and easy how to retrieve them and how to protect them.
Please check in this article - List of mandatory documents required by ISO 9001:2015 - https://advisera.com/9001academy/knowledgebase/list-of-mandatory-documents-required-by-iso-90012015/ the list of mandatory records required by ISO 9001:2015
You can find more information about records below:
You must know the standard as a whole and the interpretation and purpose of its clauses. You must have experience of working with ISO 9001 in several contexts, for example, as quality manager, as a consultant, as trainer, as auditor. You must like what you do because knowing about ISO 9001 is like a journey, you must be always in the “search mode” there is always a better interpretation, a better example, each organization is different and you should have an open mind to avoid imposing rigid or “imported” models. So, you must be aware of what others are writing and publishing. You must also develop your own brand by evidencing your knowledge. You evidence your knowledge when you write. You should write. Share what you know, share your experience and results, share testimonies of your customers about the outcomes of working with you. Use blogs, professional networks, trade magazines, use your LinkedIn profile, make presentations at conferences. And don’t forget to develop a network of contacts.
If you need an initial aid to start working in the implementation of a quality management system perhaps this course could be useful, you can enroll for free - ISO 9001:2015 Lead Implementer Course - https://advisera.com/training/iso-9001-lead-implementer-course/
If you want to become a lead auditor of quality management systems perhaps this course could be useful, you can enroll for free - ISO 9001:2015 Lead Auditor Training Course - https://advisera.com/training/iso-9001-lead-auditor-course/
If you need some ideas about starting a consulting work, perhaps this webinar can give you some ideas - Free webinar on demand – How to sell ISO consulting services - https://advisera.com/9001academy/webinar/how-to-sell-iso-consulting-services-free-webinar-on-demand/
ISO 9001:2015 does not impose extra work on organizations. ISO 9001:2015 sets requirements and it is up to each organization to decide how to apply those requirements. For example, ISO 9001:2015 requires that organizations perform quality control of its products and services - as long as legislation or regulation not prescribe what to control, how to control and when to control, it is up to each organization to decide the scope and depth of that quality control.
Benefits to company employees with the implementation of a quality management system according to ISO 9001:2015 can be about:
You can find more information about ISO 9001 below:
You can still define the whole organization in the ISMS scope, but in cases where you have physically separate sites, the most common approach, for those which goes for certification, is to separate the scope by sites (ISO 27001 accepts scope definition in terms of location, processes, business units, or information). This way, in case a site is not compliant, it does not affect the certification in the other sites.
Since you are not going for certification at this moment, you should evaluate the costs and effort involved in both approaches (i.e., centralized and decentralized scope).
1. If there is no risks from the risk treatment (thus nor risk treatment number for the control), should one use risks from the risk assessment (select risk numbers which have already treated by a control) for the justification for selection?
our assumption is correct. If you identified during the risk assessment that relevant risks are already in acceptable levels because the related control is already implemented, then you can use these risks as justification for the applicability of the control in the SoA.
For further information, see:
2. I have a hard time to figure out which are differences between secure areas (A.11.1.5) and securing offices, rooms and facilities?
Control A.11.1.5 refers to how to work on secure areas (e.g., do not use cameras inside, forbid unsupervised work, etc.), while control A.11.1.3 refers to physical controls implemented to improve the security of the environment (e.g., located away from public traffic, soundproof, etc.).
These articles will provide you a further explanation about physical security:
These materials will also help you regarding ISO 27001 controls:
For this mapping, I suggest you take a look at these templates (although they are related to ITIL, they can be applicable to ISO 27001 IT Disaster Recovery):
The first can help you as a custodian of the information about all operational services.
The second can help you record all configuration item-related data.
These articles will provide you a further explanation about service catalog and configuration management: