In today’s digital age, where businesses are increasingly reliant on technology and information, ensuring the security of sensitive data is paramount. ISO/IEC 27001:2022, the international standard for information security management systems (ISMS), provides a robust framework to help organizations safeguard their information assets. The LICQual ISO/IEC 27001:2022 Information Security Lead Implementer course is designed to equip professionals with the knowledge and skills to implement this critical standard effectively.
ISO/IEC 27001:2022 is a globally recognized standard that sets out the criteria for establishing, implementing, maintaining, and continually improving an Information Security Management System (ISMS). The standard provides a comprehensive approach to securing sensitive company information, ensuring data integrity, confidentiality, and availability. By adopting ISO/IEC 27001:2022, organizations can protect themselves from data breaches, cyberattacks, and other security threats, which are crucial in maintaining trust with customers and stakeholders.
The LICQual ISO/IEC 27001:2022 Information Security Lead Implementer course is designed for professionals who want to become proficient in establishing and managing an ISMS within their organisation. The course covers the core concepts of ISO/IEC 27001:2022, including risk management, control implementation, and continuous improvement.
In an era where information security is crucial to an organisation’s success, the LICQual ISO/IEC 27001:2022 Information Security Lead Implementer course offers a detailed and practical approach to managing information security risks. By obtaining this certification, professionals can ensure that their organisations implement the highest standards of security, comply with legal requirements, and build trust with customers and partners. If you are looking to enhance your organisation’s resilience against cyber threats and data breaches, this course is an excellent investment in your professional development and your company’s future security.
Course Overview
Qualification Title
LICQual ISO/IEC 27001:2022 Information Security Lead Implementer
Total Units
6
Total Credits
40
GLH
120
Qualification #
LICQ2200134
Qualification Specification
To enrol in the LICQual ISO/IEC 27001:2022 Information Security Lead Implementer course, applicants should meet the following criteria:
- A basic understanding of information security concepts and principles.
- Familiarity with the ISO/IEC 27001 standard or any other management system standard (though prior certification is not always mandatory).
- Experience or involvement in the implementation or management of information security practices within an organization.
- A background in IT, security management, risk management, or a related field is beneficial.
- No specific prerequisites are required, but individuals with experience in risk management, compliance, or IT security will find the course particularly valuable.
|
Qualification# |
Unit Title |
Credits |
GLH |
|---|---|---|---|
|
LICQ2200134-1 |
Introduction to ISO/IEC 27001:2022 and ISMS |
6 |
20 |
|
LICQ2200134-2 |
Leadership and Commitment in Information Security |
6 |
20 |
|
LICQ2200134-3 |
Risk Assessment and Risk Treatment |
6 |
20 |
|
LICQ2200134-4 |
Control Objectives and Controls Implementation |
6 |
20 |
|
LICQ2200134-5 LICQ2200134-6 |
Monitoring, Measurement, and Evaluation of ISMS Performance Continual Improvement of the ISMS |
8 8 |
20 20 |
By the end of this course, learners will be able to:
- Introduction to ISO 13485: Purpose, Scope, and Structure
- Understand the purpose and benefits of implementing ISO 13485 in medical device organizations.
- Identify the structure and key clauses of the ISO 13485 standard.
- Comprehend the scope of the standard and how it applies to the medical device manufacturing industry.
- Management Requirements
- Recognize the management responsibilities as outlined in ISO 13485.
- Understand the organizational structure and its role in maintaining an effective QMS.
- Develop an understanding of documentation, record-keeping, and resource management required for ISO 13485 compliance.
- Risk Management
- Understand the principles of risk management in the context of medical device manufacturing.
- Implement risk assessment, risk control, and risk communication processes as per ISO 14971.
- Develop risk management strategies for design, production, and post-market activities.
- Design and Development
- Learn to establish and manage the design and development processes for medical devices.
- Understand the requirements for design inputs and outputs, as well as the need for verification and validation.
- Gain insight into managing design changes and ensuring compliance with ISO 13485 during product development.
- Production and Service Provision
- Understand the processes involved in the production and service provision of medical devices.
- Learn how to control production processes, validate processes, and handle nonconforming products.
- Develop strategies for ensuring that products meet quality and regulatory standards throughout the production cycle.
- Post-Market Surveillance
- Learn how to implement post-market surveillance processes to monitor medical device performance after release.
- Develop a process for complaint handling, vigilance reporting, and corrective actions.
- Understand the importance of continuous improvement in response to post-market feedback and regulatory requirements.
This diploma is ideal for:
- Quality Managers: Responsible for overseeing quality assurance and quality control functions within medical device manufacturing organizations, seeking to implement and maintain ISO 13485-compliant quality management systems.
- Regulatory Affairs Managers: Ensuring compliance with regulatory requirements for medical devices, including European Medical Device Regulation (MDR) and U.S. Food and Drug Administration (FDA) Quality System Regulation (QSR).
- Product Development Managers: Overseeing the design and development of medical devices, seeking to establish processes that meet regulatory requirements and ensure product safety and effectiveness.
- Manufacturing Managers: Managing production and service provision processes within medical device manufacturing organizations, seeking to ensure product quality, reliability, and compliance with ISO 13485 requirements.
- Quality Assurance Officers: Ensuring compliance with ISO 13485 requirements, conducting internal audits, and facilitating management reviews to improve organizational effectiveness and customer satisfaction.
Assessment and Verification
All units within this qualification are subject to internal assessment by the approved centre and external verification by LICQual. The qualification follows a criterion-referenced assessment approach, ensuring that learners meet all specified learning outcomes.
To achieve a ‘Pass’ in any unit, learners must provide valid, sufficient, and authentic evidence demonstrating their attainment of all learning outcomes and compliance with the prescribed assessment criteria. The Assessor is responsible for evaluating the evidence and determining whether the learner has successfully met the required standards.
Assessors must maintain a clear and comprehensive audit trail, documenting the basis for their assessment decisions to ensure transparency, consistency, and compliance with quality assurance requirements.
