VintaBio

Cambridge, MA
No confirmed program data — ClinicalTrials.gov verification pending · Last scored 2026-09-07
59.0
Signal Score
○ FDA Inspections ○ Clinical Trials ○ SEC Filings ○ Press ○ EMA GMP ○ MHRA GMP

Quick Facts: VintaBio

Signal Score
59.0/100 (as of 2026-09-07)
Quality Compliance
Assessment pending
Headquarters
Cambridge, MA
Modalities
AAV, Lentiviral
Active Programs
Data pending
Data Sources
FDA Data Dashboard, ClinicalTrials.gov, SEC EDGAR, press monitoring
Scored By
CDMO Signal — independent CDMO intelligence platform

About VintaBio

Early-stage CGT CDMO.

Signal Score & Pillar Breakdown

Scores are being republished. Scores are being republished under methodology v3.3. The score shown is the last complete v3.2 result, which is also what directory listings and search results show. A pillar breakdown is not shown because the current one is computed under v3.3 and would not explain a v3.2 score. Regulatory evidence below is current.
Quality Compliance —
No FDA inspection records found. This CDMO may operate under a different legal name or may not have US FDA-inspected facilities.
FDA InspectionsNo US records on file
Operations —
No ClinicalTrials.gov facility matches confirmed for this manufacturer.
Programs — no verified data
Sponsors— no verified data
ModalitiesAAV, Lentiviral
Data sourced from ClinicalTrials.gov, FDA, SEC EDGAR, and verified press only. No unverified estimates shown.
Financial Stability 60.0
Profile-based financial assessment
SEC FilingsPrivate company
Capacity 58.0
Profile-based capacity assessment

Frequently Asked Questions About VintaBio

What is VintaBio's CDMO Signal Score?
VintaBio has a Signal Score of 59/100, based on quality, operations, financial stability, and capacity data.
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