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Our Editorial Criteria

Inventory Ready is a curated directory. Being listed means a company has been reviewed under our published editorial framework. This page describes those criteria, where our data comes from, and what our listings do and do not represent.

Last updated: April 25, 2026

Editorial method

Six gates, before any name appears.

This is the operating manual for the directory. If a vendor appears here, every gate below was cleared. If you spot a case where it wasn’t, write to the editor and we’ll publish the correction.

  1. Evidence

    Capability claims confirmed by ≥1 independent source.

    What it means in practice

    • FDA Data Dashboard
    • NSF / SQF / UL public directories
    • ThomasNet listings
    • Trade press 2024 to 2026
    • Operator references

    If unmet

    We don’t list. The method protects the directory’s integrity for everyone in it.

  2. Freshness

    Reviewed within 12 months. Re-checked after FDA actions.

    What it means in practice

    • Profile timestamps every section
    • Watchlist for warning letters
    • Quarterly re-pull of inspection data

    If unmet

    We don’t list. The method protects the directory’s integrity for everyone in it.

  3. Provenance

    Every fact has a citation. Click it.

    What it means in practice

    • CFR section numbers, not paraphrase
    • Inspection records linked at source
    • Certificates confirmed at issuer

    If unmet

    We don’t list. The method protects the directory’s integrity for everyone in it.

  4. Challenge

    Vendor sees draft. Can correct facts, not framing.

    What it means in practice

    • 7-day window for corrections
    • Disagreements published in §8 of the profile
    • Editor decides framing

    If unmet

    We don’t list. The method protects the directory’s integrity for everyone in it.

  5. Disclosure

    Commercial relationship printed at the top of every profile.

    What it means in practice

    • Profile fee, never per-lead
    • No paid placement
    • Affiliate links labeled in CFR style

    If unmet

    We don’t list. The method protects the directory’s integrity for everyone in it.

  6. Abstention

    When evidence is incomplete, we wait. Empty beats wrong.

    What it means in practice

    • Re-review on schedule when new data is published
    • Vendor invited to provide missing documentation
    • No editorial commentary on absence

    If unmet

    We don’t list. The method protects the directory’s integrity for everyone in it.

Method · v1.4 · Last updated April 25, 2026 · Editor: Greg Huang

What Our Comparisons Represent

Our comparison pages present factual, publicly available information about service providers within the same category. They are organized by specific criteria (such as minimum order quantity range or certification status) so that buyers can evaluate options based on their own priorities.

Our assessments and comparisons represent Inventory Ready's editorial opinions based on publicly available information. They are not certifications, audits, endorsements, or guarantees. Like a rating agency's credit opinion, our assessments reflect a structured evaluation process applied to available data. They are opinions informed by evidence, not statements of fact about a manufacturer's operations.

What Our Comparisons Are Not

  • Not rankings. The order of manufacturers on comparison pages reflects the stated organizing criteria (alphabetical, by MOQ, by certification count), not a quality judgment.
  • Not recommendations. We present data. You make the decision. We strongly recommend visiting any facility before signing a manufacturing agreement.
  • Not complete. Our dataset covers 189 manufacturers across 8 categories. Many qualified manufacturers are not yet in our directory.
  • Not static. Manufacturer capabilities, certifications, and operations change. Our listings reflect information available at the time of last review.

Comparison Criteria

Each comparison page states its organizing criteria. We compare manufacturers on factual attributes where data is available:

CriterionWhat We ReportData Source
CertificationsEach certification is labeled as confirmed (found in independent database), self-reported (claimed but not independently confirmed), or not independently confirmedNSF, USP, SQF public directories; manufacturer websites
Minimum order quantityReported as stated by the manufacturer. Ranges are noted when exact figures are unavailableManufacturer websites, ThomasNet, direct inquiry
Lead timeTypical production lead time as stated by the manufacturer. Actual lead times may vary by product complexity and seasonManufacturer websites, direct inquiry
Dosage formsWhich product forms the manufacturer produces (capsules, tablets, powders, gummies, softgels, liquids, etc.)Manufacturer websites, product catalogs
LocationCity and state of primary manufacturing facilityFDA registration, company websites
CapabilitiesServices offered beyond manufacturing (formulation, packaging, design, fulfillment, etc.)Manufacturer websites, service descriptions

Inclusion Criteria

Each category is evaluated against criteria appropriate to its regulatory and professional context. Our review considers applicable compliance requirements, verifiable capabilities, and public documentation. The specific criteria vary by service type: a contract manufacturer's regulatory landscape differs from a fulfillment provider's or a testing lab's.

All categories share baseline editorial standards: no unresolved FDA enforcement actions, no known fraud indicators, public documentation exists, and at least one verifiable capability claim.

Category-specific criteria: Different vendor types operate under different regulatory and professional contexts. Contract manufacturers are evaluated against cGMP compliance and FDA facility registration requirements. Testing laboratories are evaluated against ISO/IEC 17025 accreditation scope. Fulfillment providers are evaluated against food safety certifications and FDA registration for dietary supplement holding. Packaging and labeling providers are evaluated against supplement packaging experience and relevant quality certifications. The specific criteria for each category are documented in our internal evaluation frameworks.

Large companies (conglomerate threshold): Companies with total revenue exceeding $5 billion undergo the same editorial criteria as all other vendors, plus a supplement-relevance assessment. To qualify, a large company must have named, branded ingredients or services marketed specifically to dietary supplement manufacturers; an identifiable US market presence serving supplement brands; and supplement-specific trade press coverage or trade event participation. This ensures that our directory remains focused on the dietary supplement supply chain.

Criteria may evolve as our editorial approach develops. We are a small editorial team; our review depth is described honestly, and not every listed company has received identical scrutiny.

Data Sources and Verification

All manufacturer information is sourced from publicly available records. We do not conduct on-site inspections or audits. Each manufacturer listing cites its specific sources so readers can verify our work.

Our primary data sources include: company websites, FDA registration databases, third-party certification directories (NSF International, USP, SQF), industry databases (ThomasNet), state business registries, and manufacturer-provided documentation. We also cross-reference OpenFDA enforcement databases for recalls and warning letters.

When we confirm a third-party certification, we verify that the manufacturer appears in the certifying body's current public directory. This confirms the certification is active as of our review date. This does not constitute an independent assessment of the manufacturer's regulatory compliance. Certification verification and regulatory compliance are evaluated through separate processes in our assessment framework. A confirmed certification reflects the certifying body's listing status; enforcement records, warning letters, and inspection history are reviewed independently through FDA databases.

When information conflicts between sources, we note the discrepancy. When information is unavailable from public sources, we do not speculate or make assumptions.

Assessment Principles

Every manufacturer in our directory is assessed using the same six-gate editorial framework. The gates ensure consistency in how we gather, evaluate, and present information. For a full description of each gate, see our How We Assess page.

  • Evidence

    Claims backed by documentation

  • Freshness

    Reviewed within the last 12 months

  • Provenance

    Sources cited for every claim

  • Challenge

    Inconsistencies flagged, not hidden

  • Disclosure

    Material connections stated

  • Abstention

    Unknown = not published

Editorial Independence

No manufacturer can pay for a better position on comparison pages or for a more favorable assessment. Our comparison comparison method and assessment criteria are the same for every manufacturer, regardless of any commercial relationship. For full details on our revenue model, see How We Get Paid.

How We Work

AI tools assist our research and drafting process. We use AI-assisted analysis to gather publicly available information, cross-reference data sources, and identify inconsistencies. All assessments are reviewed and finalized by Greg Huang, founder of multiple consumer brands in the dietary supplement and nutrition industry since 2009. We disclose AI usage because transparency about process is as important as transparency about data.

Certifications and other claims in manufacturer profiles are confirmed as of the date shown on each profile. Certification status can change after our review. We do not continuously monitor manufacturer credentials. Always confirm current certifications directly with any manufacturer you are evaluating.

More broadly, every element of a company profile reflects information available at the time of our review. This includes trust tier assignment, editorial evaluation, inclusion criteria review, and assessment notes. The “Last reviewed” date on each profile marks when this snapshot was taken. We do not continuously monitor listed companies. Always confirm current status directly with any company you are evaluating before making decisions.

Limitations

  • Our dataset is limited to manufacturers we have assessed. Many qualified manufacturers are not yet in our directory.
  • We rely on publicly available information. Manufacturers may have capabilities, certifications, or issues not reflected in public records.
  • Our assessment is point-in-time. Manufacturers change. Certifications lapse or are earned. Facilities expand or close.
  • We are not a regulatory body. Our assessments do not replace FDA inspection, third-party audits, or your own due diligence.

Manufacturer Participation

Manufacturers not yet in our directory can request a review for inclusion. Listed manufacturers can request corrections, provide additional documentation, or ask to be removed at any time through our Claim or Update a Listing page. Corrections supported by documentation are reviewed and incorporated. Manufacturer participation does not influence assessment outcomes.

Correction Policy

Factual accuracy is the foundation of everything we publish. When we get something wrong, we fix it publicly.

  • Report an error. Use our Claim or Update a Listing form, or email us directly. Include the specific information you believe is incorrect and the documentation supporting the correction.
  • Investigation. We review reported errors within 7 business days. If the error is confirmed, we update the listing immediately. If the reported information conflicts with our sources, we note the discrepancy on the profile.
  • Published corrections. Substantive corrections (incorrect certification status, wrong location, erroneous capability claims) are noted with the date of correction and a brief description of what changed. Minor corrections (typos, formatting) are made without notation.

Editorial Status Tiers

Every vendor listing has an editorial status that reflects the depth of our review. This is separate from the commercial status (whether the manufacturer has opted into any paid features).

StatusMeaningWhat it includes
Source-CheckedInformation reviewed against public recordsAll claims cross-referenced with cited sources. Certifications labeled as confirmed or self-reported. Editorial inclusion criteria checked against our published framework.
AssessedFull editorial assessment completedSource-checked plus: all six editorial gates applied, assessment rationale written, FDA enforcement database cross-referenced.

Two-Axis Trust Model

Every vendor profile has two independent status indicators. Editorial status reflects our review depth. Commercial status reflects whether the vendor has opted into paid features. These are independent: a paid vendor does not get a better editorial assessment.

AxisWhat it measuresValues
EditorialDepth and rigor of our independent reviewSource-Checked, Assessed
CommercialWhether the vendor has a commercial relationshipBasic (free listing), Confirmed, Partner

A vendor with “Basic” commercial status and “Assessed” editorial status has no commercial relationship with us but has been fully reviewed. A vendor with “Partner” commercial status and “Source-Checked” editorial status has a disclosed commercial relationship but has only been partially reviewed. The editorial assessment is the same regardless of commercial tier.

Trust Tiers

Every vendor listing displays a trust badge that reflects the depth of verification we have completed. Trust tiers are organized into three groups. Each tier adds exactly one verifiable layer of diligence beyond the tier below it.

Trust tiers reflect our verification depth, not a quality judgment. A higher tier means we have completed more verification steps, not that the vendor is “better.” Vendors progress through tiers as additional verification is completed.

Directory Listing

Baseline inclusion in our curated directory. All listed vendors were reviewed under our published editorial framework.

ListedVendor was reviewed under editorial inclusion criteria and published in our directory.
Records ReviewedPublic records and independent sources have been reviewed and cross-referenced.
Certifications ConfirmedOne or more certifications independently confirmed through public certification body registries.

IR Assessed

Deeper verification including enforcement records review and full editorial assessment.

Enforcement Records ReviewedFDA enforcement databases, inspection classifications, and warning letter archives reviewed. No unresolved adverse findings identified in our review.
Assessment CompleteFull editorial assessment completed, including all six editorial gates and detailed assessment rationale.

IR Vetted

The highest level of review, involving direct engagement with the vendor and ongoing monitoring.

References ValidatedCustomer references contacted and independently confirmed.
Operations ReviewedFacility operations reviewed through virtual or on-site walkthrough.
IR Vetted PartnerFull vetting program completed with ongoing monitoring agreement.

These vetting tiers are part of our planned assessment roadmap. No vendors have reached this level yet.

Trust badges do not represent endorsements, certifications, or guarantees. They describe the verification steps Inventory Ready has completed. Always conduct your own due diligence before entering into any business relationship.

Sample Assessment Walkthrough

To illustrate how our assessment process works, here is a summary of how we evaluated Gemini Pharmaceuticals, a contract manufacturer in Commack, New York. Gemini has no commercial relationship with Inventory Ready.

Evidence

8 certifications claimed on website and marketing materials (cGMP, FDA Registered, Health Canada, TGA, NSF, ISO 17025, Non-GMO Project, Organic/QAI). We searched publicly accessible databases for each. Certifications found in independent databases are labeled confirmed; those not found are labeled self-reported. Each certification on the profile shows its verification status.

Freshness

All information sourced from records reviewed in March 2026. Sources include the company website, Suffolk County IDA public filings ($25M expansion), and certification databases.

Provenance

Each claim on the profile links to its source. The expansion figure ($25M, 75 jobs) traces to Suffolk County IDA public records.

Challenge

Lead time and MOQ are not publicly disclosed. Certifications that could not be confirmed through independent databases are labeled self-reported rather than assumed accurate.

Disclosure

All material connections are disclosed on affected listings and on our How We Get Paid page.

Abstention

We did not conduct an on-site inspection. This limitation is stated on the profile. The 300,000-unit MOQ may be a consideration for smaller brands evaluating this manufacturer.

This is the same process applied to every manufacturer in our directory. The depth of the assessment varies by editorial status tier, but the framework is consistent.

Dietary supplement manufacturers must comply with 21 CFR Part 111 (Current Good Manufacturing Practice for dietary supplements). This includes requirements for personnel, facilities, equipment, production, laboratory operations, and record-keeping.

See Our Method in Practice

Browse compared manufacturers and see how this framework applies to real listings.