BioReliance (Merck)

Glasgow, UK · Rockville, MD
Hybrid — also manufactures internal programs
Program data pending ClinicalTrials.gov matching · Last scored 2026-03-15
65.5
Signal Score
✓ FDA Inspections (1) ○ Clinical Trials ○ SEC Filings ○ Press

Quick Facts: BioReliance (Merck)

Signal Score
65.5/100 (as of 2026-03-15)
Quality Compliance
Assessment pending
Headquarters
Glasgow, UK · Rockville, MD
Modalities
AAV, Lentiviral, Biologics
Active CGT Programs
No ClinicalTrials.gov matches confirmed
Data Sources
FDA Data Dashboard, ClinicalTrials.gov, SEC EDGAR, press monitoring
Scored By
CDMO Signal — independent CGT manufacturing intelligence platform

Signal Score & Pillar Breakdown

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 Inspections1 on record
Warning Letters0
Last InspectionVoluntary Action Indicated (VAI) (2024-11-22)
Operations
No ClinicalTrials.gov facility matches confirmed for this manufacturer.
Programs no verified data
Sponsorsno verified data
ModalitiesAAV, Lentiviral, Biologics
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 68.0
Parent company: Merck KGaA
Financial assessment: 68.0/100
Source: SEC EDGAR, press monitoring
Subsidiary of Merck KGaA
SEC FilingsParent: Merck KGaA
Parent company: Merck KGaA
Financial assessment: 68.0/100
Capacity 63.0
2 CGT manufacturing sites
Sites: Glasgow, UK, Rockville, MD
Source: SEC EDGAR, press monitoring, company profiles
2 CGT manufacturing sites
2 CGT manufacturing sites

FDA Inspection History

2024-11
NAI VAI OAI
Date Site Type Observations Classification
2024-11-22 Rockville, Maryland Vaccines and Allergenic Products Yes Voluntary Action Indicated (VAI)
Source: FDA Data Dashboard · Retrieved Mar 20, 2026
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