Biopharma CDMO intelligence
Find manufacturing partners. Know what to ask next.
Search CDMOs against your program’s needs. Examine the evidence, see what still needs confirming, and — once your search takes shape — keep a sourcing brief you can refine and share.
Search and preview free, no account Verify your work email to keep a brief
See how it worksHow it helps
See what’s evidenced. Ask about the rest.
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Evidenced, or only claimed
Each manufacturer we track is compared with your needs on public evidence — regulatory records, and third-party records of what they make — kept apart from what suppliers say about themselves.
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The right questions
Each gap becomes a specific question for that manufacturer, so supplier calls start where the evidence stops.
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A decision you can share
Once your search takes shape, keep your shortlist, your reasoning and the open questions in one sourcing brief, and share a read-only copy with your team.
You need
Microbial fermentation at an EU site
- Manufacturer A Evidenced at site A third-party record ties this process to a named EU site
- Manufacturer B Claimed only The supplier describes it; no record ties it to a site
- Manufacturer C Not evidenced Nothing we hold establishes it
Ask Manufacturer B
“At which site would you run microbial fermentation for this program, and what capacity and track record does that site have?”
Built on public regulatory and clinical records
- CDMOs tracked
- 162
- FDA inspections
- 627
- EMA GMP certificates
- 371
- MHRA GMP certificates
- 166
- Clinical studies
- 31,551
Also SEC EDGAR filings and press monitoring. Manufacturers can’t pay to influence scores. How the evidence is read →