Pharmaron Biologics
San Diego, CA · Shaoxing, China, Liverpool, UK, Ningbo China
Program data pending ClinicalTrials.gov matching
· Last scored 2026-07-28
86.9
Signal Score
✓ FDA Inspections (3)
○ Clinical Trials
○ SEC Filings
✓ Press (1)
○ EMA GMP
○ MHRA GMP
Quick Facts: Pharmaron Biologics
- Signal Score
- 86.9/100 (as of 2026-07-28)
- Quality Compliance
- 100.0/100 — Bonus: 3 consecutive NAI inspections
- Headquarters
- San Diego, CA · Shaoxing, China, Liverpool, UK, Ningbo China
- Modalities
- AAV, Lentiviral, Plasmid, mAb, Antibody, Recombinant Protein, Biosimilars
- Active Programs
- No ClinicalTrials.gov matches confirmed
- Data Sources
- FDA Data Dashboard, ClinicalTrials.gov, SEC EDGAR, press monitoring
- Scored By
- CDMO Signal — independent CDMO intelligence platform
About Pharmaron Biologics
Chinese CRO/CDMO with US CGT operations.
Signal Score & Pillar Breakdown
Quality Compliance
100.0
Bonus: 3 consecutive NAI inspections
Source: FDA Data Dashboard
Bonus: 3 consecutive NAI inspections
FDA Inspections3 on record
Warning Letters0
Last InspectionNo Action Indicated (NAI) (2025-07-17)
Bonus: 3 consecutive NAI inspections
Operations
—
No ClinicalTrials.gov facility matches confirmed for this manufacturer.
Programs
— no verified data
Sponsors— no verified data
ModalitiesAAV, Lentiviral, Plasmid, mAb, Antibody, Recombinant Protein, Biosimilars
No clinical trial matches found for this manufacturer
Operational score requires ClinicalTrials.gov data
Data sourced from ClinicalTrials.gov, FDA, SEC EDGAR, and verified press only. No unverified estimates shown.
Financial Stability
83.0
Publicly traded — financial transparency
Source: SEC EDGAR, press monitoring
Profile-based financial assessment
SEC FilingsPrivate company
Publicly traded — financial transparency
Capacity
68.0
2 manufacturing sites
Broad modality coverage (7 modalities)
Sites: San Diego, CA, Shaoxing, China, Liverpool, UK, Ningbo China
Source: SEC EDGAR, press monitoring, company profiles
2 manufacturing sites
StatusAvailable
2 manufacturing sites
Broad modality coverage (7 modalities)
Sites: San Diego, CA, Shaoxing, China, Liverpool, UK, Ningbo China
Recent Press1 articles
2 manufacturing sites
Broad modality coverage (7 modalities)
Pharmaron Biologics FDA Inspection History
2025-07
2025-01
2024-09
NAI
VAI
OAI
| Date | Site | Type | Observations | Classification |
|---|---|---|---|---|
| 2025-07-17 | Coventry, Rhode Island | Drug Quality Assurance | No | No Action Indicated (NAI) |
| 2025-01-17 | Exton, Pennsylvania | Human Cellular, Tissue, and Gene Therapies | No | No Action Indicated (NAI) |
| 2024-09-27 | Exton, Pennsylvania | Bioresearch Monitoring | No | No Action Indicated (NAI) |
Source: FDA Data Dashboard · Retrieved Aug 22, 2026
Recent News 1 articles
How HTPD transforms AAV process optimization and scale-up - News-Medical
Frequently Asked Questions About Pharmaron Biologics
How many FDA inspections does Pharmaron Biologics have on record?
CDMO Signal tracks 3 FDA inspections for Pharmaron Biologics, sourced from the FDA inspection database. See the full inspection history above.
Has Pharmaron Biologics received an FDA warning letter?
CDMO Signal has no FDA warning letters on record for Pharmaron Biologics.
What is Pharmaron Biologics's CDMO Signal Score?
Pharmaron Biologics has a Signal Score of 87/100, based on quality, operations, financial stability, and capacity data.
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