Industry Perspectives
Analysis and curated insights on systemic risk, emerging threats, and the evolving healthcare risk landscape.
Top Risks in Medical Device Supply Chains
Analysis of 10 failure points in medical device supply chains and immediate actions to reduce shortages, cyber and quality risks.
Read Post >>South Korea watchdog unveils AI safety framework for finance
South Korea’s Financial Security Institute unveils an AI reliability and safety evaluation framework for finance.
Read Post >>Baylor Genetics reports breach affecting patient, employee data
Law firm investigates Baylor Genetics data breach exposing patient and employee personal information.
Read Post >>Lone Star Community Health breach exposes 250,130 patients
Law firm investigates Lone Star Community Health Center breach exposing 250,130 patients' personal and medical data.
Read Post >>HIPAA Compliance and DLP: What You Need to Know
How DLP supports HIPAA: monitor, log, and control ePHI (email, endpoints, cloud) while pairing tools with risk analysis and governance.
Read Post >>NIST CSF for IoT: Key Metrics to Track
Five IoT incident-response metrics—MTTD, MTTA/MTTR-start, containment, recovery, improvement—mapped to NIST CSF for safer device operations.
Read Post >>AI in Third-Party Risk Scoring Models
AI should triage and continuously update healthcare vendor risk, but final high‑impact decisions must remain human‑controlled.
Read Post >>How EDR Enhances Threat Containment in Real Time
EDR stops attacks fast in healthcare by isolating devices, blocking harmful behavior, and matching automation to patient-safety needs.
Read Post >>Ultimate Guide to Risk-Based Compliance in Clinical Software
Prioritize testing and controls for functions that can harm patients, expose ePHI, or disrupt care; validate and maintain risk evidence.
Read Post >>HIPAA Audit Logging in Forensic Analysis
How to make HIPAA audit logs forensic-ready: standard fields, centralized immutable storage, six-year retention, and documented review.
Read Post >>Common Compliance Gaps in Medical Device Security
Five compliance gaps: incomplete inventory, weak patching/SBOMs, poor access, unclear ownership, and thin logging raise medical device risk.
Read Post >>AI Vendor Accountability Standards in Healthcare
Six practical rules to vet, contract, validate, monitor, and suspend healthcare AI vendors to protect patients and PHI.
Read Post >>Data Flow Analysis vs. Threat Modeling in Healthcare
Map where ePHI flows, then threat-model those paths to rank risks, protect patient safety, and meet HIPAA requirements.
Read Post >>SOC 2, HIPAA, PCI DSS: Mapping Compliance with Tools
Compare five compliance tools and learn where shared controls cut redundant work across SOC 2, HIPAA, and PCI DSS.
Read Post >>Common Root Causes of Healthcare Cybersecurity Incidents
Most healthcare breaches start with staff-targeted attacks and persist due to legacy systems, weak identity controls, and vendor risk.
Read Post >>How HITECH Act Impacts Healthcare Cybersecurity
Explains HITECH's breach-notice rules, security safeguards, vendor liability, risk analysis, and enforcement evidence.
Read Post >>Medical Device Wireless Security vs. Wired Systems
Wireless vs wired medical device risks: RF interception/jamming vs LAN, USB and port threats; mitigate with encryption and segmentation.
Read Post >>Checklist: Choosing Encryption for Data-at-Rest in Healthcare
Practical checklist to encrypt PHI at rest: AES-256, key management, algorithm choices, testing, and risk controls.
Read Post >>Medical Device Threat Monitoring: FDA Expectations
FDA-aligned approach: central device inventory, SBOM mapping, unified alert intake, risk-based triage, and tested response playbooks.
Read Post >>Cloud Security Monitoring for Medical Devices
Medical device security must extend into the cloud — monitor device, network, API, cloud, and PHI flows with centralized logs and patient-risk-based response.
Read Post >>AI in Cyber Threat Detection for Emergency Systems
AI speeds cyber threat detection across ED, EMS, EHR and medical devices while keeping human review for high-impact actions.
Read Post >>5 Steps for Post-Market Cybersecurity Disclosure
A five-step workflow for handling medical device cybersecurity: intake, validation, remediation, disclosure, and documented closure.
Read Post >>Cyberattack Playbooks for Medical Devices
Compare four playbooks—hospital, manufacturer, coordination, and FDA guidance—to prepare for and respond to medical device cyberattacks.
Read Post >>Ultimate Guide to Incident Response for Emergency Care
Actionable incident response guidance for ED and EMS: patient-safety focused downtime plans, roles, containment, recovery, and HIPAA documentation.
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