Blog / GRC

Business Continuity and Disaster Recovery Plan: template, requirements, and audit evidence for 2026

Business continuity and disaster recovery plan guide for 2026: required sections, owners, implementation steps, and audit evidence for SOC 2 and ISO 27001.

BYOD Policy: template, requirements, and audit evidence for 2026

BYOD policy guide for 2026: required sections, owners, implementation steps, and audit evidence for SOC 2, ISO 27001, and enterprise security reviews.

Change Management Policy: template, requirements, and audit evidence for 2026

Change management policy guide for 2026: required sections, owners, implementation steps, and audit evidence for SOC 2, ISO 27001, and security reviews.

Code of Conduct Policy: template, requirements, and audit evidence for 2026

Code of conduct policy guide for 2026: required sections, owners, implementation steps, and audit evidence for SOC 2, ISO 27001, and security reviews.

Cryptography Policy: template, requirements, and audit evidence for 2026

Cryptography Policy guide for 2026: required sections, owners, implementation steps, and audit evidence for SOC 2, ISO 27001, and enterprise security reviews.

Data Management Policy: template, requirements, and audit evidence for 2026

Data Management Policy guide for 2026: required sections, owners, implementation steps, and audit evidence for SOC 2, ISO 27001, and security reviews.

Data Retention Policy: template, requirements, and audit evidence for 2026

Data retention policy guide for 2026: required sections, owners, implementation steps, and audit evidence for SOC 2, ISO 27001, and enterprise security reviews.

EU Cyber Resilience Act SBOM requirements: what product makers must do

EU Cyber Resilience Act SBOM requirements: who is in scope, what the CRA demands, key deadlines, and how to build a compliant SBOM process before 2027.

Executive Order 14028 and SBOMs: what software vendors must know

Executive Order 14028 SBOM requirements explained: OMB memos, CISA attestation forms, NTIA minimum elements, and what selling software to US agencies takes.

FDA SBOM requirements for medical devices: a Section 524B guide

FDA SBOM requirements explained: Section 524B, cyber device definitions, premarket submission expectations, and how device makers build a compliant process.