Results for “device-compliance”

Classify medical devices under EU MDR 2017/745, build technical documentation, plan clinical evaluations, and manage post-market surveillance and EUDAMED integration.

Configure Microsoft Entra ID (Azure AD) Conditional Access policies for zero trust access control, covering signal-based policy design, device compliance, risk-based authentication, named locations, session controls, and NIST SP 1800-35 integration.

Orchestrates multi-framework compliance programs by selecting applicable frameworks, mapping control overlaps, simulating audits, and consolidating evidence checklists.

Restricts unauthorized removable media access on endpoints by implementing USB device control policies via Group Policy, Intune, or EDR platforms to prevent data exfiltration and malware introduction.

Enforces GDPR-compliant deployment practices for Google Cloud Run, including Frankfurt region verification, PII-safe logging, data anonymization, retention policies, and CSP configuration.

Routes compliance requests to the appropriate regulatory and quality-management skill among 15 bundled options, covering ISO 13485, EU MDR, FDA submissions, ISO 14971, CAPA, document control, ISO 27001, ISO 42001, EU AI Act, GDPR, SOC 2, and auditing.

Guides implementation of data protection and privacy controls for regulatory frameworks such as GDPR, HIPAA, SOC 2, and PCI-DSS, including audits, retention policies, and data subject requests.

Implement PCI DSS 4.0.1 compliance controls across all 12 requirements, including scoping, network security, data protection, access controls, monitoring, and governance.

Reference for SOC 2, PCI-DSS, HIPAA, and GDPR compliance requirements, including control checklists, evidence collection, and audit preparation guidance.

Categorize BES cyber systems and implement NERC CIP compliance controls for high, medium, and low impact assets, including electronic security perimeters, configuration management, and supply chain risk management.

Provides ISO 13485 internal audit methodology for medical device quality management systems, covering audit planning, execution, nonconformity classification, and external audit preparation.

Prepares for FDA QSR audits by asking six forcing questions covering complaints, process validation, DHRs, CAPAs, labeling, and Form 483 history.

Enforce identity verification, device compliance, and data protection for cloud-hosted services using CASB, SSPM, conditional access policies, OAuth app governance, and session controls.