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    CDMOHUBCDMOHUB
    Pricing
    CDMOHUB

    Connecting biotech and pharma teams with verified manufacturing partners worldwide.

    Platform

    • Find CDMOs
    • CDMO Matchmaking
    • Expert Matchmaking
    • Modality Guides
    • Supplier Maps
    • Join as Partner

    Company

    • Blog
    • Briefings
    • About Us
    • Contact

    Legal

    • Terms of Service
    • Privacy Policy

    © 2026 CDMOHUB. All rights reserved.

    CDMO Hub, Inc. Registered in Delaware, USA

    CDMOHUBCDMOHUB
    Pricing
    1. Home
    2. /Rankings
    3. /Cell & Gene Therapy CDMOs

    Best Cell & Gene Therapy CDMOs, ranked by FDA evidence

    Last updated August 4, 2026 · Evidence Score formula v1.0

    We don’t yet have enough verified public regulatory evidence to rank this category

    We publish a ranked list only when we can stand behind every number in it. For cell & gene therapy cdmos we are not there yet, so we are showing you nothing rather than showing you a list we cannot defend.

    Why this page is empty

    • Below the evidence threshold. 0 companies in this category have an FDA inspection record we can verify against a source. We require at least 10 before publishing a ranked list. A shorter list padded with unverifiable records would be worse than no list.
    Browse all biologics CDMOs

    Our eligibility gates and the evidence we require are published in full on our ranking methodology.

    Frequently Asked Questions

    How is this ranking calculated?+
    Companies are ranked on an Evidence Score built from three public-FDA-sourced dimensions: regulatory evidence (45%), approved-product record (30%), and modality-match depth (25%). A dimension with no evidence is withheld and the remaining weights renormalize — an absence is never scored as a zero. The full rubric, the eligibility gates, and the tie-break order are published on our methodology page.
    Can a CDMO pay to appear higher on this list?+
    No. Featured placement, partner tier, verification status, reviews, profile completeness, subscription tier, and profile views are not read by the ranking query or the scorer. Nothing a seller can pay for or self-report is an input to the rank.
    What does NAI, VAI, or OAI mean on an FDA inspection?+
    They are the FDA’s post-inspection classifications. NAI (No Action Indicated) means the inspection closed without objectionable conditions being cited. VAI (Voluntary Action Indicated) means objectionable conditions were found but did not warrant regulatory action. OAI (Official Action Indicated) means regulatory action was warranted. NAI is a classification, not a clean bill of health.
    Why are some companies missing from this list?+
    A company appears only when its FDA record is verifiable: real per-inspection history, an FEI facility identifier, and a verified ingestion timestamp. A profile carrying an inspection count we cannot trace to an FDA record is excluded rather than estimated, even when that means a shorter list.
    Is the Evidence Score enough to choose a manufacturing partner?+
    No. The FDA record is one input. It does not capture technical fit, capacity availability, project-management quality, or anything a site audit would surface. Use this list to build a shortlist, then do your own technical and quality due diligence.
    CDMOHUB

    Connecting biotech and pharma teams with verified manufacturing partners worldwide.

    Platform

    • Find CDMOs
    • CDMO Matchmaking
    • Expert Matchmaking
    • Modality Guides
    • Supplier Maps
    • Join as Partner

    Company

    • Blog
    • Briefings
    • About Us
    • Contact

    Legal

    • Terms of Service
    • Privacy Policy

    © 2026 CDMOHUB. All rights reserved.

    CDMO Hub, Inc. Registered in Delaware, USA