Pharmaron Biologics

San Diego, CA · Shaoxing, China, Liverpool, UK, Ningbo China
Claimed Profile AAV Lentiviral Plasmid mAb Antibody Recombinant Protein Biosimilars
No confirmed program data — ClinicalTrials.gov verification pending · Last scored 2026-09-07
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 2026-09-07)
Quality Compliance
100.0/100
Headquarters
San Diego, CA · Shaoxing, China, Liverpool, UK, Ningbo China
Modalities
AAV, Lentiviral, Plasmid, mAb, Antibody, Recombinant Protein, Biosimilars
Active Programs
Data pending
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

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 100.0
FDA Inspections3 on record
Warning Letters0
Last InspectionNo Action Indicated (NAI) (2025-07-17)
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
Data sourced from ClinicalTrials.gov, FDA, SEC EDGAR, and verified press only. No unverified estimates shown.
Financial Stability 83.0
Profile-based financial assessment
SEC FilingsPrivate company
Capacity 68.0
Capacity status: Available
StatusAvailable
Recent Press1 articles

Pharmaron Biologics FDA Inspection History

2025-07
2025-01
2024-09
NAI VAI OAI
Date Site Type Observations Classification
2025-07-17
Pharmaron Manufacturing Services (US) LLC
Coventry, Rhode Island Facility-linked
Drug Quality Assurance No No Action Indicated (NAI)
2025-01-17
Pharmaron (Exton) Lab Services LLC
Exton, Pennsylvania Facility-linked
Human Cellular, Tissue, and Gene Therapies No No Action Indicated (NAI)
2024-09-27
Pharmaron (Exton) Lab Services LLC
Exton, Pennsylvania Facility-linked
Bioresearch Monitoring No No Action Indicated (NAI)
Source: FDA Data Dashboard · Retrieved Oct 07, 2026

Recent News 1 articles

news Fri, 09 Ja
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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