Industry Perspectives

Analysis of rising pharma cyberattacks, breach causes, forensic methods, and steps to protect R&D, supply chains, and patient data.

Summary of 2026 HIPAA/FDA encryption mandates: AES-256 for data at rest, TLS 1.2+ for transit, legacy controls, and compliance steps.

A structured HIPAA incident response plan is essential to protect ePHI, meet 60‑day breach deadlines, and reduce operational risk.

HDO primer on FDA's 2025 cybersecurity labeling: 14 required elements, SBOMs, update commitments, and end-of-support risks.

Align ISO 27001 risk assessments with healthcare goals using SMART objectives, cross-department input, continuous reviews, and automation.

Third-party libraries in medical devices pose security and compliance risks; SBOMs, automated scans, and monitoring reduce exposure.

Premarket cybersecurity checklist for medical devices: threat modeling, SBOMs, secure design, testing, and FDA-ready documentation.

Guide to AES-256, FIPS 140-3, and automated RiskOps for securing PHI at rest, with key management and HIPAA compliance.

Use frameworks, KPIs, and automated tools to reduce vendor, device, and patient-data risks in healthcare IT.

Telehealth demands rigorous risk frameworks to protect patient data, secure cloud services, and hold vendors accountable.

Healthcare supply chains are the weakest link in patient data protection, with vendors and devices creating major breach risks.

How HDOs can secure third‑party libraries in medical devices using SBOMs, automated scanning, lifecycle monitoring, and FDA-aligned processes.

Guidelines for HIPAA-compliant cloud audit trails: centralized, tamper-proof logging, PHI minimization, encryption, and regular reviews.

Steps to securely erase PHI from medical devices using NIST 800-88 methods, verification, and compliant vendor practices.

Steps, techniques and tools to de-identify PHI, meet HIPAA, and balance privacy with data utility for healthcare research.

How to discover, track, secure, and govern healthcare IoT devices to reduce breaches, ensure compliance, and cut downtime.

SMART on FHIR OAuth 2.0 standardizes discovery, scopes, PKCE, and token handling to secure and streamline EHR app access.

One year after enforcement, the PATCH Act requires SBOMs, 30-day patches, and lifecycle security while revealing major legacy device risks.

A concise 6-step process to identify ePHI risks, prioritize remediation, and document HIPAA Security Rule compliance.

HIPAA vs HITRUST: legal rules vs voluntary certification—key differences, costs, and when to use each for protecting healthcare data.

ISO 27701:2025 explains how healthcare organizations can protect patient data, manage AI/IoT risks, and simplify privacy audits.

Step-by-step HITECH risk analysis: define ePHI scope, assess threats, prioritize risks, implement safeguards, and document monitoring.

Overview of FDA SBOM rules for Class II/III medical device suppliers, required SBOM elements, timelines, and postmarket updates.

Clear summary of 2026 PHI retention rules: HIPAA's six-year compliance requirement, federal and state record timelines, and disposal best practices.