Cross-Framework Mapping

21 CFR Part 58 — Good Laboratory Practice (GLP)vsCISA ICS-CERT Advisories and Industrial Control Systems Security Guidelines

See exactly how 21 CFR Part 58 — Good Laboratory Practice (GLP) controls map to CISA ICS-CERT Advisories and Industrial Control Systems Security Guidelines. Pre-computed mappings, identified gaps, and coverage analysis.

5
Controls Mapped
26
Gaps Found
10%
Coverage

According to the TheArtOfService Compliance Knowledge Graph:

21 CFR Part 58 — Good Laboratory Practice (GLP) maps to CISA ICS-CERT Advisories and Industrial Control Systems Security Guidelines with 10% coverage across 3 directly mapped controls. Analysis of 31 21 CFR Part 58 — Good Laboratory Practice (GLP) controls identifies 28 compliance gaps — primarily concentrated in Test Articles and Protocol (Subparts F & G).

Source: TheArtOfService Knowledge Graph | 31 controls analysed | 693 frameworks | 819K+ cross-framework mappings

Control Mappings

Showing 5 of 5 mapped controls across 2 domains. Sign up to explore all 819K+ mappings across 693 frameworks.

General Provisions (Subpart A)(4 mappings)

58.1Scope2 targets
FEDRAMP-AC-1Access Control Policy and Procedures
FEDRAMP-AC-2Account Management
58.3Definitions2 targets
FEDRAMP-AC-1Access Control Policy and Procedures
FEDRAMP-AC-2Account Management

Facilities (Subpart C)(1 mappings)

58.43Animal Care Facilities
ICS-AC-4Physical access controls

Related Comparisons

Other 21 CFR Part 58 — Good Laboratory Practice (GLP) comparisons

Other CISA ICS-CERT Advisories and Industrial Control Systems Security Guidelines comparisons

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What are the key differences between 21 CFR Part 58 — Good Laboratory Practice (GLP) and CISA ICS-CERT Advisories and Industrial Control Systems Security Guidelines?

21 CFR Part 58 — Good Laboratory Practice (GLP) has 31 controls across its framework, while CISA ICS-CERT Advisories and Industrial Control Systems Security Guidelines covers 42 controls. Direct mapping analysis identifies 3 overlapping controls (10% coverage). The frameworks diverge most significantly in Test Articles and Protocol (Subparts F & G), where 5 21 CFR Part 58 — Good Laboratory Practice (GLP) controls have no direct CISA ICS-CERT Advisories and Industrial Control Systems Security Guidelines equivalent.

How many controls map between 21 CFR Part 58 — Good Laboratory Practice (GLP) and CISA ICS-CERT Advisories and Industrial Control Systems Security Guidelines?

Of 31 total 21 CFR Part 58 — Good Laboratory Practice (GLP) controls, 3 map directly to CISA ICS-CERT Advisories and Industrial Control Systems Security Guidelines controls — representing 10% coverage. The remaining 28 controls represent compliance gaps requiring additional documentation or compensating controls to satisfy both frameworks simultaneously.

What are the compliance gaps when mapping 21 CFR Part 58 — Good Laboratory Practice (GLP) to CISA ICS-CERT Advisories and Industrial Control Systems Security Guidelines?

28 21 CFR Part 58 — Good Laboratory Practice (GLP) controls have no direct equivalent in CISA ICS-CERT Advisories and Industrial Control Systems Security Guidelines. The highest concentration of gaps is in Test Articles and Protocol (Subparts F & G) with 5 unmapped controls. These gaps represent areas where additional controls, policies, or documentation must be created to achieve compliance with both frameworks.

Which control domains have the most gaps between 21 CFR Part 58 — Good Laboratory Practice (GLP) and CISA ICS-CERT Advisories and Industrial Control Systems Security Guidelines?

The domain with the highest gap count is Test Articles and Protocol (Subparts F & G) (5 gaps). Export the full domain-by-domain gap breakdown via the Professional tier to generate a prioritised remediation roadmap.

This platform provides educational compliance tools, not legal, regulatory, or professional compliance advice. Cross-framework mappings are AI-assisted interpretations and do not reproduce or replace official standards. Framework names and trademarks belong to their respective owners. Consult qualified professionals for your specific compliance requirements. See our Terms of Service.