Cross-Framework Mapping

PIC/S Guide to Good Manufacturing Practice for Medicinal ProductsvsNIST SP 800-171A Rev 3 - Assessing CUI Security Requirements

See exactly how PIC/S Guide to Good Manufacturing Practice for Medicinal Products controls map to NIST SP 800-171A Rev 3 - Assessing CUI Security Requirements. Pre-computed mappings, identified gaps, and coverage analysis.

22
Controls Mapped
0
Gaps Found
67%
Coverage

According to the TheArtOfService Compliance Knowledge Graph:

PIC/S Guide to Good Manufacturing Practice for Medicinal Products maps to NIST SP 800-171A Rev 3 - Assessing CUI Security Requirements with 67% coverage across 6 directly mapped controls. Analysis of 9 PIC/S Guide to Good Manufacturing Practice for Medicinal Products controls identifies 3 compliance gaps — primarily concentrated in Self Inspection.

Source: TheArtOfService Knowledge Graph | 9 controls analysed | 718 frameworks | 332K+ cross-framework mappings

Control Mappings

Showing 20 of 22 mapped controls across 6 domains. Sign up to explore all 332K+ mappings across 718 frameworks.

Pharmaceutical Quality System(3 mappings)

PICSGMP-1Chapter 1: Pharmaceutical Quality System (PQS) and Quality Risk Management3 targets
3.1Physical Security
3.16System and Services Acquisition
3.17Supply Chain Risk Management

Personnel(3 mappings)

PICSGMP-2Chapter 2: Personnel - Qualified Personnel, Key Responsibilities, Training3 targets
3.3Configure Data Access Control Lists
FEDRAMP-CM-6Configuration Settings
FEDRAMP-CP-9System Backup

Premises and Equipment(3 mappings)

PICSGMP-3Chapter 3: Premises and Equipment - Design, Qualification, Calibration3 targets
3.1Physical Security
3.2Establish and Maintain a Data Inventory
3.4Enforce Data Retention

Documentation(4 mappings)

PICSGMP-4Chapter 4: Documentation - System, Record-Keeping, Data Integrity4 targets
3.1Physical Security
3.2Establish and Maintain a Data Inventory
3.3.1Audit Record Creation
3.4Enforce Data Retention

Production(3 mappings)

PICSGMP-5Chapter 5: Production Operations and Material Management3 targets
3.3Configure Data Access Control Lists
FEDRAMP-CM-6Configuration Settings
FEDRAMP-CP-9System Backup

Outsourced Activities(4 mappings)

PICSGMP-7Chapter 7: Outsourced Activities and Supplier Management4 targets
3.16System and Services Acquisition
3.17Supply Chain Risk Management
3.3Configure Data Access Control Lists
3.5Securely Dispose of Data

+2 more mappings

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Related Comparisons

Other PIC/S Guide to Good Manufacturing Practice for Medicinal Products comparisons

Other NIST SP 800-171A Rev 3 - Assessing CUI Security Requirements comparisons

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What are the key differences between PIC/S Guide to Good Manufacturing Practice for Medicinal Products and NIST SP 800-171A Rev 3 - Assessing CUI Security Requirements?

PIC/S Guide to Good Manufacturing Practice for Medicinal Products has 9 controls across its framework, while NIST SP 800-171A Rev 3 - Assessing CUI Security Requirements covers 35 controls. Direct mapping analysis identifies 6 overlapping controls (67% coverage). The frameworks diverge most significantly in Self Inspection, where 1 PIC/S Guide to Good Manufacturing Practice for Medicinal Products controls have no direct NIST SP 800-171A Rev 3 - Assessing CUI Security Requirements equivalent.

How many controls map between PIC/S Guide to Good Manufacturing Practice for Medicinal Products and NIST SP 800-171A Rev 3 - Assessing CUI Security Requirements?

Of 9 total PIC/S Guide to Good Manufacturing Practice for Medicinal Products controls, 6 map directly to NIST SP 800-171A Rev 3 - Assessing CUI Security Requirements controls — representing 67% coverage. The remaining 3 controls represent compliance gaps requiring additional documentation or compensating controls to satisfy both frameworks simultaneously.

What are the compliance gaps when mapping PIC/S Guide to Good Manufacturing Practice for Medicinal Products to NIST SP 800-171A Rev 3 - Assessing CUI Security Requirements?

3 PIC/S Guide to Good Manufacturing Practice for Medicinal Products controls have no direct equivalent in NIST SP 800-171A Rev 3 - Assessing CUI Security Requirements. The highest concentration of gaps is in Self Inspection with 1 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 PIC/S Guide to Good Manufacturing Practice for Medicinal Products and NIST SP 800-171A Rev 3 - Assessing CUI Security Requirements?

The domain with the highest gap count is Self Inspection (1 gaps). Export the full domain-by-domain gap breakdown via the Professional tier to generate a prioritised remediation roadmap.

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