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Gap Analysis

What is Gap Analysis?

A comparison between an organisation's current state and the requirements of a target framework or standard. Identifies areas that need improvement to achieve compliance.

Compliance

Each of these is named in at least one of the same controls as gap analysis. The number is how many controls name both.

What the standards actually require on gap analysis

Requirements naming gap analysis across 6 standards, quoted from the control text.

COBIT 20192 controls

The differences between the current and the target environment are found and the broad changes to the enterprise architecture are described. Every gap and every change required to reach the target is identified;

cobit-2019::APO02.04 · APO02.04 Conduct a gap analysis →

Based on the legacy software's safety class, the manufacturer performs a gap analysis of the available deliverables against those clauses 5.2, 5.3, 5.7 and 7 require, assesses the continuing validity of what exists, evaluates for each gap the risk reduction fr...

iec-62304-2015-medical-device-software-lifecycle-processes::4.4.3 · 4.4.3 Gap analysis →

The organization should form a planning team of the key people in A.2.2 to develop, run, maintain and improve the plan, each knowing their own and the others' roles in planning, response and recovery, and should assign the following.

ansi-asis-wvpi-aa-2020-workplace-violence-and-active-assailant::A.2.3 · A.2.3 Identify responsibilities and authorities of key personnel →

TRANSITION PATH from prior QSR to QMSR: the FDA Final Rule (89 FR 7496) provides a 2-year implementation period - the QMSR applies from 2 FEBRUARY 2026 + manufacturers must fully implement the harmonised QMSR by that date.

QMSR-Transition · Transition from prior QSR + 2 February 2026 application + FDA inspection approach →
HKMA TM-G-11 control

HKMA TM-G-1 implementation roadmap + status. ORGANIZATIONAL ROLES at AI: (a) BOARD + RISK COMMITTEE - TM-G-1 governance oversight + Technology Risk Management Framework approval + Risk Appetite + Pillar 2;

HKMA-TMG1-Implementation-Roles-Tooling-Status · TM-G-1 Implementation Roadmap, Roles, Tooling, Status and Future →

An Operations Manual contains the policies, processes and procedures ground handling personnel need and its current edition is usable at every location;

iata-operational-safety-audit-iosa-standards-manual::GRH 1.6 · GRH 1.6 Operational Manuals →

Questions people ask about gap analysis

What is Gap Analysis?
A comparison between an organisation's current state and the requirements of a target framework or standard. Identifies areas that need improvement to achieve compliance.
Why is Gap Analysis important for compliance?
Gap Analysis is a key concept in Compliance. Understanding gap analysis helps organizations meet regulatory requirements, reduce risk, and demonstrate due diligence during audits. Our compliance platform maps 1,016 frameworks with 316K cross-framework control mappings.
Which compliance frameworks address Gap Analysis?
Gap Analysis appears in the requirement text of COBIT 2019, IEC 62304:2015 Medical Device Software Lifecycle Processes, ANSI/ASIS WVPI AA-2020 Workplace Violence and Active Assailant, FDA Quality Management System Regulation (QMSR), HKMA TM-G-1. Across these standards we have identified 8 controls that name it directly, each linked to the control text on the compliance platform.
Where can I learn more about Gap Analysis?
Explore our compliance framework pages to see how gap analysis applies across different standards and regulations. Our implementation guides provide step-by-step guidance, and the compliance platform offers AI-powered analysis of how this concept maps across 1,016 frameworks.

See how Gap Analysis applies across compliance frameworks

Our platform maps 1,016 frameworks with 316K cross-framework control mappings. Explore how this concept is addressed across standards.

Written and maintained by Gerard Blokdyk, The Art of Service.