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Impact Genome Registry

LinkedIn lists Chicago, Illinois as headquarters.

What it is

Impact Genome Registry standardizes social program outcomes so nonprofits can report impact and funders can evaluate programs. Its standards link programs to one or more of 132 outcomes across areas including education, public health, human needs, and arts and culture. The Registry describes its coverage as more than 2.2 million global nonprofits and social programs. Programs self-report data, and the verification process uses information they already collect rather than requiring new data collection. Trained verifiers assess annual claims and supporting evidence through standardized protocols; reporting typically covers the most recent program cycle. Verified programs can receive a Verified Impact Report and Verified Impact Units representing positive social outcomes. Nonprofit membership includes a consultation, a shareable annual report, benchmarking, research tools, webinars, and ongoing support. Funder tools include charity search, impact forecasting, and portfolio analysis. The free self-reporting option is not evaluated by in-house experts. Nonprofit membership costs $1,000, paid once, billed per program.

For and against

For

  • Standards cover 132 social outcome areas
  • Free self-reporting option is available
  • Verification uses data programs already collect
  • Funders can access search and portfolio tools
  • Membership includes benchmarking and research tools

Against

  • Free self-reported outcomes are not evaluated by in-house experts
  • Nonprofit membership costs $1,000, paid once per program
  • Benchmarks are typically not published with fewer than five verified reports

The verdict

Impact Genome Registry offers a shared outcome framework, with expert verification available through nonprofit membership. Funders have tools for charity search and portfolio analysis, while free self-reporting does not include in-house expert evaluation.

Who it suits

The Registry is for nonprofits and social enterprises reporting program outcomes, as well as funders seeking portfolio data and insights. Its free self-reporting option may suit organizations that do not need expert evaluation.

Plans and prices

Registry self-reporting

Free

Self-reported outcomes; no in-house evaluation

Impact producer membership

$1,000usage-based

Verification · Impact Verified Scorecard · expert guidance

Nonprofit membership

$1,000one-time

Verification by evaluation experts · Impact Verified Scorecard · expert guidance

Funder Registry subscription

Priced on request

Aggregate portfolio reports · year-over-year trends · strategy insights

Every plan, in full

On the record

API access
Philanthropy Data Solutions lists API access as custom-priced rather than universally free.philanthropydatasolutions.org · read 14 Oct 2026
API availability
Read/write APIs are reported as available only for select partners.philanthropydatasolutions.org · read 14 Oct 2026
Benchmarking limit
The maker says it typically does not publish an outcome benchmark when fewer than five verified reports are available.impactgenome.com · read 7 Oct 2026
Benchmark limitation
Benchmarks usually are not published when fewer than five verified reports exist for an outcome.impactgenome.com · read 14 Oct 2026
Charity matching
Funder subscriptions can search more than 2.2 million nonprofits by outcomes, SDGs, beneficiary traits and location.impactgenome.com · read 14 Oct 2026
Collaboration
Organizations can add unlimited users, pause and resume submissions, and clone prior reports for later years.impactgenome.com · read 14 Oct 2026
Company legal name
Crunchbase identifies Mission Metrics, LLC as the legal name behind Impact Genome Corp.crunchbase.com · read 14 Oct 2026
Company size
LinkedIn lists 11–50 employees.linkedin.com · read 14 Oct 2026
Company status
Crunchbase lists the company as private and active.crunchbase.com · read 14 Oct 2026
Data collection
Program data is self-reported, and the maker says its verification process works with data programs already collect without requiring new data collection.impactgenome.com · read 7 Oct 2026
Data limitation
Household-income data is not currently captured, and the company says it does not customize functionality for each funder.impactgenome.com · read 14 Oct 2026
Data portability
Nonprofits can download reports and data at no charge and generate shareable reports and PDFs.philanthropydatasolutions.org · read 14 Oct 2026
Developer documentation
The directory says SDKs, sandboxes and developer guides were created with partners, rather than documenting a broadly public toolkit.philanthropydatasolutions.org · read 14 Oct 2026
Founded history
The company says its work began in 1994 with the Center for What Works and later produced the Impact Genome Project and Registry.impactgenome.com · read 14 Oct 2026
Funder tools
The funder subscription page describes charity search, impact forecasting, and portfolio analysis tools.impactgenome.com · read 7 Oct 2026
Funding support
Impact Genome says its work is backed by the Gates Foundation and the Chan Zuckerberg Initiative.impactgenome.com · read 14 Oct 2026
Geographic benchmark limitation
Published cost-per-outcome benchmarks combine programs across regions and interventions; granular regional benchmarks are still being developed.impactgenome.com · read 14 Oct 2026
Guided workflow
The verification intake uses existing program data, guided questions and evidence attachments without requiring new data collection.impactgenome.com · read 14 Oct 2026

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