Pass Using ISO-22301-Lead-Auditor Exam Dumps

The clarify and confirm step is the first step of the audit planning process, where the auditor clarifies the requirements with the business leads, such as the audit client, the auditee, and the audit team. The purpose of this step is to ensure that the audit objectives, scope, criteria, and deliverables are clearly defined, understood, and agreed upon by all the parties involved. The clarify and confirm step also involves the identification of the audit risks, opportunities, and resources, as well as the establishment of the audit communication channels and protocols. The clarify and confirm step is essential to ensure that the audit is aligned with the expectations and needs of the stakeholders, and that the audit is feasible, effective, and efficient. References:

• PECB Certified ISO 22301 Lead Auditor eLearning Training Course1, Module 4: Preparation of an ISO 22301 audit, Lesson 4.1: Audit planning, Slide 5: Audit planning process
• ISO 22301 Auditing eBook2, Chapter 4: Preparation of an ISO 22301 audit, Section 4.1: Audit planning, Subsection 4.1.1: Clarify and confirm

The step that collates and validates all resource requirements of the selected continuity solutions is the compile step. This step involves gathering all the information about the resources needed to implement and operate the continuity solutions, such as human resources, equipment, facilities, materials, suppliers, partners, etc. The compile step also involves verifying that the resource requirements are realistic, feasible, and consistent with the organization’s objectives, policies, and budget1.

References: 1: ISO 22301 Auditing eBook, Chapter 6: Business Continuity Strategy, Section 6.2: Continuity Solutions, Subsection 6.2.4: Compile, Page 88.

 A control is a measure that is implemented to reduce or eliminate the risk from occurring, or to mitigate the impact of the risk if it occurs. A control can be preventive, corrective, or detective, depending on the stage of the risk management process. A control can also be administrative, technical, or physical, depending on the nature of the risk and the organization. A control can be designed, implemented, monitored, and evaluated based on the risk assessment and the risk treatment plan. A control can be documented in the business continuity policy, objectives, plans, procedures, and other relevant documents. A control can be audited to verify its effectiveness and efficiency in achieving the intended outcomes. References:

• PECB Certified ISO 22301 Lead Auditor eLearning Training Course1, Module 3: Fundamental principles and concepts of a business continuity management system (BCMS), Lesson 3.2: Business continuity management system (BCMS), Slide 15: Risk management
• ISO 22301 Auditing eBook2, Chapter 3: Fundamental principles and concepts of a business continuity management system (BCMS), Section 3.2: Business continuity management system (BCMS), Subsection 3.2.4: Risk management

The Statement of Applicability (SOA) is a document that identifies the applicable requirements of ISO 22301 and explains how they are addressed by the organization’s Business Continuity Management System (BCMS). The SOA is prepared during the planning phase of the PDCA cycle, as part of the process of establishing the BCMS scope, objectives, and policy. The SOA is based on the results of the business impact analysis, risk assessment, and risk treatment, and it provides a rationale for the inclusion or exclusion of each requirement. The SOA also helps to demonstrate the conformity of the BCMS with the standard and to communicate the BCMS scope and objectives to interested parties. References: ISO 22301:2019, Clause 6.1.3; ISO 22301 Auditing eBook, Chapter 4.2.2.