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Product: Conformio Product: ISO 27001 Documentation Toolkit Product: ISO 13485 & MDR Integrated Documentation Toolkit ISO 27001 Product: ISO 27001 & ISO 22301 Premium Documentation Toolkit ISO 9001 Risk Assessment Product: ISO 13485 Documentation Toolkit ISMS Internal Audit register of requirements Product: ISO 27001/Risk Assessment Table Product: ISO 27001 & ISO 27017 & ISO 27018 Cloud Documentation Toolkit AS9100 Product: EU GDPR Documentation Toolkit
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  • Certification ISO 27001

    How long must a sgsi (ISMS) be operating to pass the certification process

  • Measures and Metrics

    We have been struggling to get our measures and metrics right. Is there any best practice or education around measures and metrics?

  • How to control data tape movement during COVID19

    We are ISO certified organization and due to COVID 19, we are not able to comply controls i.e. backup tapes movement from one location to off-site location

    How do we address this? Is there any advisory published by ISO / any template /format where we can mention this and take approval from management & it will be helpful during the audit as well.

  • Corrective actions

    How an auditor can verify that agreed corrective actions have been effectively implemented?

  • Internal Audit - choice of auditor

    Is it typical in smaller companies (50-100 employees) that for the internal audit an external auditor is being hired?  Or should you be thinking of somebody internally in the first place anyhow?

  • Business Continuity Policy 22301

    1. I'm reading the Business continuity Policy according to ISO 22301; I Don't understand why it is written, "Because in many cases the executives have no idea how business continuity can help their organization, which means they won’t be particularly interested in supporting the business continuity effort in their company."
    How it can be possible?

    2. If they are not involved that plant will be closed?

  • 8.1 Operational planning and control

    Since the Clause itself says “The organization shall keep documented information to the extent necessary to have confidence that the processes have been carried out as planned.”, does the Document in your Toolkit “Project Plan” fulfills the requirement of this clause? Since we will be planning the different phases of ISMS implementation in this doc and carrying out accordingly, do we require any other Documented info as it is a mandatory Doc to avoid major non Conformity.

  • BCP and DR

    Hello, I am having a hard time understanding the difference between BCP and DR.  I know for our ISO cert we have to include a.17.4.6 right?  That is the Disaster Recovery Plan, but our certifier is saying we do not have to complete the Business Continuity Plan, which is the rest of a.17, why is that?

  • Is there any process flow chart available that can be used for an audit process?

    Many thanks for offering the Lead Auditor ISO27001, I was wondering if one has to start an audit, is there any process chart that can be used as guide ( like a flow chart ) 

    Define Scope --> Review ISP and related documents --> Perfrom SOA --> etc

    Something similar to Diagram of ISO27001 Implementation process but for conducting an audit 

    Cheers

    Alex

  • Questions about risk

    Whilst attending your ISO/IEC 27001 Lead implementer course, the following question (which actually consists of two subquestions) has arisen:

    After risk assessment (in which I have considered also already implemented controls in order to reduce likelihood and/or impact) I still have a small number of unacceptable risks (i.e. with high-risk level).
    Now I have to choose between available risk treatment options. I decide to apply further controls (although I think I could also choose risk acceptance as a risk treatment option and as a result to simply live with risks due to my risk appetite). I pick up 2-3 applicable controls (although there are more applicable controls in Annex A which I do now wish to adopt) from Annex A which will be implemented in the risk treatment plan later on.

    First subquestion: Is my thinking process aligned with ISO/IEC 27001 requirements?

    Second subquestion: I now have to create the statement of applicability. Can I only consider (in the SoA) those controls which I have considered as significant for reducing my unacceptable risks OR is it mandatory to implement also controls (from Annex A) which I regard (according to my opinion) as not really useful or which I simply do not wish to apply?
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