Agilent Technologies (Oligo GMP)
Santa Clara, CA
Reagent / Material Supplier
1 confirmed programs
· 1 sponsors
· Last scored 2026-04-29
74.2
Signal Score
✓ FDA Inspections (2)
✓ Clinical Trials (1)
○ SEC Filings
○ Press
○ EMA GMP
○ MHRA GMP
Quick Facts: Agilent Technologies (Oligo GMP)
- Signal Score
- 74.2/100 (as of 2026-04-29)
- Quality Compliance
- 100.0/100
- Headquarters
- Santa Clara, CA
- Modalities
- Oligonucleotide
- Active Programs
- 1 confirmed from ClinicalTrials.gov across 1 sponsors
- Data Sources
- FDA Data Dashboard, ClinicalTrials.gov, SEC EDGAR, press monitoring
- Scored By
- CDMO Signal — independent CDMO intelligence platform
About Agilent Technologies (Oligo GMP)
Reagent/raw material supplier.
Signal Score & Pillar Breakdown
Quality Compliance
100.0
FDA Inspections2 on record
Warning Letters0
Last InspectionNo Action Indicated (NAI) (2026-05-06)
Operations
60.0
1 active programs across 1 sponsors
Modalities: Oligonucleotide
1 programs in advanced phases (Phase 2/3)
Source: ClinicalTrials.gov
1 active programs across 1 sponsors · Modalities: Oligonucleotide · 1 programs in advanced phases (Phase 2/3)
Programs
1
Sponsors1
ModalitiesOligonucleotide
1 active programs across 1 sponsors
Modalities: Oligonucleotide
1 programs in advanced phases (Phase 2/3)
Source: ClinicalTrials.gov facility matching
Source: ClinicalTrials.gov · Retrieved Jul 04, 2026
Financial Stability
68.0
Parent company: Agilent Technologies
Financial assessment: 68.0/100
Source: SEC EDGAR, press monitoring
Profile-based financial assessment
SEC FilingsPrivate company
Parent company: Agilent Technologies
Financial assessment: 68.0/100
Capacity
53.0
1 manufacturing site: Boulder, CO
Modalities: Oligonucleotide
Capacity assessment: 53.0/100
Sites: Boulder, CO
Source: SEC EDGAR, press monitoring, company profiles
1 manufacturing site
1 manufacturing site: Boulder, CO
Modalities: Oligonucleotide
Capacity assessment: 53.0/100
Agilent Technologies (Oligo GMP) FDA Inspection History
2026-05
2025-06
NAI
VAI
OAI
| Date | Site | Type | Observations | Classification |
|---|---|---|---|---|
| 2026-05-06 | Boulder, Colorado | Drug Quality Assurance | No | No Action Indicated (NAI) |
| 2025-06-18 | Frederick, Colorado | Drug Quality Assurance | No | No Action Indicated (NAI) |
Source: FDA Data Dashboard · Retrieved Jul 04, 2026
Clinical Activity 1 studies
Source: ClinicalTrials.gov · Retrieved Jul 04, 2026
Frequently Asked Questions About Agilent Technologies (Oligo GMP)
How many FDA inspections does Agilent Technologies (Oligo GMP) have on record?
CDMO Signal tracks 2 FDA inspections for Agilent Technologies (Oligo GMP), sourced from the FDA inspection database. See the full inspection history above.
Has Agilent Technologies (Oligo GMP) received an FDA warning letter?
CDMO Signal has no FDA warning letters on record for Agilent Technologies (Oligo GMP).
How many clinical programs is Agilent Technologies (Oligo GMP) linked to?
Agilent Technologies (Oligo GMP) is associated with 1 clinical trial in CDMO Signal's ClinicalTrials.gov-sourced data.
What is Agilent Technologies (Oligo GMP)'s CDMO Signal Score?
Agilent Technologies (Oligo GMP) has a Signal Score of 74/100, based on quality, operations, financial stability, and capacity data.
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