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Information Security Controls Assessment in ISO 27799

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What does the Information Security Controls Assessment in ISO 27799 course cover?

Information Security Controls Assessment in ISO 27799 is covered here in 10 modules: Scoping and Context Definition for Healthcare Information Assets, Risk Assessment Methodology Aligned with ISO 27799, Access Control Design for Clinical and Administrative Roles and 7 more. The outline lists 80 specific topics, opening with determine which systems, applications, and data stores fall within the scope of ISO 27799 based.

How do you approach Information Security Controls Assessment in ISO 27799 step by step?

The work is sequenced in 10 stages. It starts with Scoping and Context Definition for Healthcare Information Assets, moves through Risk Assessment Methodology Aligned with ISO 27799 and Access Control Design for Clinical and Administrative Roles, and ends at Governance Integration and Executive Reporting. Each stage carries its own topic list, so the sequence is followed rather than summarised.

What is in Module 1 of the Information Security Controls Assessment in ISO 27799 course?

Module 1 is Scoping and Context Definition for Healthcare Information Assets. It works through determine which systems, applications, and data stores fall within the scope of ISO 27799 based on patient data handling and regulatory exposure., map ownership of clinical, administrative, and research data to accountable roles across departments such as HIM, IT, and compliance., negotiate scope boundaries with legal and clinical.

How is the Information Security Controls Assessment in ISO 27799 course delivered?

The Information Security Controls Assessment in ISO 27799 course is fully self-paced with immediate online access after enrolment. Access does not expire and future updates are included at no cost. It can be taken on any device, and a certificate of completion is issued by The Art of Service when you finish.

How much does the Information Security Controls Assessment in ISO 27799 course cost?

The Information Security Controls Assessment in ISO 27799 course is $346 as a one time payment. There is no subscription, no per seat licence and no hidden fee. Enrolment carries a 30 day satisfied or refunded guarantee, so it can be assessed in full before you commit.

Closely related courses: Information Assets Assessment, Information Lifecycle Assessment, Information Security Risk Assessment Toolkit, Information Technology in Vulnerability Assessment Dataset.

More answers: what you get with every course, refund policy, all help answers.

This curriculum spans the breadth and rigor of a multi-phase security assessment program, equivalent to an organization’s end-to-end effort to align clinical information systems with ISO 27799, from scoping and risk modeling through governance reporting.

Module 1: Scoping and Context Definition for Healthcare Information Assets

  • Determine which systems, applications, and data stores fall within the scope of ISO 27799 based on patient data handling and regulatory exposure.
  • Map ownership of clinical, administrative, and research data to accountable roles across departments such as HIM, IT, and compliance.
  • Negotiate scope boundaries with legal and clinical stakeholders when legacy systems lack audit capabilities but process PHI.
  • Classify data sensitivity levels (e.g., psychotherapy notes vs. billing records) to align with ISO 27799 control applicability.
  • Document jurisdictional overlaps where multiple regulations (HIPAA, GDPR, PIPEDA) apply to the same dataset.
  • Define exclusion justifications for outsourced services (e.g., cloud email) and ensure they are formally recorded and reviewed annually.
  • Integrate organizational risk appetite into scoping decisions, particularly when expanding telehealth platforms with third-party vendors.
  • Establish criteria for re-scoping triggered by mergers, new EHR implementations, or changes in regulatory enforcement patterns.

Module 2: Risk Assessment Methodology Aligned with ISO 27799

  • Select a risk assessment framework (e.g., OCTAVE, NIST SP 800-30) that supports healthcare-specific threat modeling, such as insider threats in clinical settings.
  • Identify threat actors specific to healthcare, including disgruntled staff, business associates with broad access, and ransomware actors targeting downtime.
  • Quantify impact using clinical harm scenarios (e.g., delayed treatment due to inaccessible records) in addition to financial and reputational metrics.
  • Adjust likelihood ratings based on observed control deficiencies in peer healthcare organizations during industry benchmarking.
  • Validate risk scenarios with clinical staff to ensure technical threats reflect real-world workflow disruptions.
  • Document residual risks that exceed tolerance levels and require escalation to the privacy and security steering committee.
  • Ensure risk assessment outputs directly inform control selection in subsequent modules, avoiding generic checklists.
  • Schedule risk reassessment triggers tied to significant events such as EHR upgrades or data center migrations.

Module 3: Access Control Design for Clinical and Administrative Roles

  • Implement role-based access control (RBAC) models that reflect clinical hierarchies (e.g., attending vs. resident) and non-clinical job functions.
  • Enforce least privilege by reviewing actual access logs and comparing them to role definitions during access certification cycles.
  • Design emergency access procedures that allow override access while ensuring real-time logging and post-event review.
  • Integrate Just-In-Time (JIT) access for third-party vendors supporting imaging systems or lab interfaces.
  • Address shared account usage in nursing stations by deploying session-level logging and user tagging at login.
  • Define access revocation timelines for terminated or transferred employees, synchronized with HR offboarding systems.
  • Configure dynamic access policies based on context, such as time-of-day restrictions for non-urgent data exports.
  • Test access control effectiveness through simulated insider threat exercises with red team participation.

Module 4: Asset Management and Data Lifecycle Controls

  • Maintain an up-to-date inventory of medical devices (e.g., infusion pumps, MRI machines) with embedded systems that process PHI.
  • Assign custodianship for data at each lifecycle stage, from collection at registration desks to archival in long-term repositories.
  • Define retention periods for different record types (e.g., adult vs. pediatric) in accordance with state and federal mandates.
  • Implement automated data aging rules in EHR systems to flag records eligible for archival or deletion.
  • Secure decommissioning of storage media containing PHI using NIST 800-88 sanitization standards and verification logs.
  • Track portable devices (e.g., loaner tablets for home health) through asset management systems with geolocation and remote wipe capability.
  • Enforce encryption requirements for data in transit between facilities, particularly when using public networks for teleradiology.
  • Conduct periodic data minimization audits to identify and purge unnecessary PHI stored in shadow systems or personal drives.

Module 5: Third-Party Risk Management in Healthcare Ecosystems

  • Assess business associate agreements (BAAs) for compliance with HIPAA and alignment with ISO 27799 control objectives.
  • Perform on-site assessments of cloud service providers hosting EHR modules, focusing on segregation and breach notification processes.
  • Require evidence of penetration testing and vulnerability management from medical device manufacturers with remote support access.
  • Implement continuous monitoring of third-party access logs, especially for billing and coding vendors with batch data extraction rights.
  • Negotiate audit rights in contracts to enable validation of security controls during the relationship lifecycle.
  • Map third-party services to critical care pathways to prioritize risk treatment for vendors supporting life-critical systems.
  • Enforce multi-factor authentication for all external users accessing internal clinical systems, regardless of BAA status.
  • Establish incident escalation protocols with joint response roles defined for breaches involving third-party systems.

Module 6: Incident Response and Breach Management Specific to PHI

  • Define criteria for classifying incidents involving PHI based on data type, volume, and potential for misuse (e.g., insurance fraud).
  • Integrate incident response playbooks with clinical operations to manage EHR outages without compromising patient care.
  • Activate breach notification workflows within 72 hours when unencrypted PHI is involved, per HIPAA requirements.
  • Preserve chain-of-custody for forensic evidence collected from clinical workstations during insider threat investigations.
  • Coordinate with legal counsel to determine whether a breach requires reporting to HHS, state regulators, and affected individuals.
  • Conduct post-incident reviews that include clinical leadership to assess workflow impact and prevent recurrence.
  • Simulate ransomware scenarios that encrypt patient records and evaluate recovery time objectives against clinical tolerances.
  • Maintain a centralized incident register that correlates events across SIEM, helpdesk, and compliance tracking systems.

Module 7: Physical and Environmental Security in Clinical Settings

  • Secure server rooms and data closets in hospitals with dual-factor access and video surveillance, considering 24/7 operational needs.
  • Install privacy filters on workstations in shared clinical areas such as emergency departments and nurses’ stations.
  • Enforce clean desk policies for work areas handling printed patient records, with daily audits in billing and registration.
  • Protect mobile devices used in home health with tamper-resistant cases and mandatory check-in/check-out procedures.
  • Design HVAC and power redundancy for data centers supporting real-time clinical decision support systems.
  • Control access to medical imaging archives stored on physical media with biometric entry and visitor logs.
  • Assess risks of patient or visitor access to unattended workstations during family visitation hours.
  • Validate physical security controls during disaster recovery drills that simulate site unavailability.

Module 8: Security Awareness and Role-Specific Training for Healthcare Staff

  • Develop phishing simulation campaigns using healthcare-themed lures (e.g., fake lab results, vaccine updates) to measure susceptibility.
  • Deliver role-based training modules for clinicians, coders, and IT staff emphasizing their unique control responsibilities.
  • Track completion rates and assessment scores for mandatory training, with escalation to supervisors for non-compliance.
  • Integrate security reminders into EHR login banners for high-risk actions such as mass download or external sharing.
  • Conduct tabletop exercises with department heads to practice responding to social engineering attempts.
  • Measure behavior change through audits of password posting, USB drive usage, and screen locking habits.
  • Update training content quarterly based on emerging threats observed in peer institutions or ISAC reports.
  • Engage clinical champions to model secure behaviors and reinforce messaging during team huddles and staff meetings.

Module 9: Audit, Monitoring, and Continuous Control Validation

  • Configure SIEM rules to detect anomalous access patterns, such as after-hours record reviews by non-treating staff.
  • Schedule quarterly control testing for critical safeguards, including access reviews, backup restoration, and firewall rule audits.
  • Integrate automated compliance checks into CI/CD pipelines for healthcare applications undergoing upgrades.
  • Perform independent audits of privilege escalation requests to verify approval trail completeness and business justification.
  • Use data loss prevention (DLP) tools to monitor and block unauthorized transfers of PHI via email or cloud storage.
  • Validate encryption status of databases and endpoints through agent-based scanning and centralized reporting.
  • Report control effectiveness metrics to the board using healthcare-specific KPIs, such as mean time to detect insider threats.
  • Adjust monitoring thresholds based on seasonal variations in clinical activity, such as flu season or system migrations.

Module 10: Governance Integration and Executive Reporting

  • Align ISO 27799 control objectives with enterprise risk management frameworks used by the executive team.
  • Present security metrics in context of clinical outcomes, such as impact on patient throughput during system outages.
  • Document control gaps and remediation plans in formats suitable for audit committees and board-level review.
  • Coordinate with privacy officers to ensure consistency between security controls and HIPAA compliance reporting.
  • Integrate findings from external audits and OCR investigations into the governance decision-making cycle.
  • Establish escalation paths for unresolved risks that exceed delegated authority levels within the security team.
  • Facilitate quarterly governance meetings with clinical, legal, and IT leadership to review control performance.
  • Link control investment decisions to strategic initiatives such as value-based care programs or population health platforms.