Commercial-Scale Gene Therapy CDMOs

Region: USA Europe Asia
35
CDMOs tracked
35
Fully scored
16
With FDA records
63
FDA inspections
250
EMA/MHRA GMP certs
2
Warning letters

Gene therapy is delivered through viral vectors — AAV, lentiviral, and adenoviral being the three dominant platforms. AAV dominates in vivo systemic delivery (rare disease, ophthalmology, neurology); lentivirus is the workhorse for ex vivo cell engineering including CAR-T; adenoviral vectors remain relevant for vaccines and select gene therapy programs. Most gene therapy CDMOs specialize in one or two vector platforms, and platform experience is the first filter in any sponsor's shortlist.

The ranking below aggregates every CDMO tracked as a gene therapy manufacturer across these platforms. For platform-specific rankings, use the dedicated pages: <a href="/modality/aav">AAV CDMOs</a>, <a href="/modality/lentiviral">Lentiviral Vector CDMOs</a>, <a href="/modality/adenoviral">Adenoviral Vector CDMOs</a>. For sponsors evaluating end-to-end programs that combine vector manufacturing with downstream cell processing, the <a href="/modality/cell-and-gene-therapy">cell and gene therapy view</a> extends this list with cell therapy CDMOs.

FDA inspection outcomes across these CDMOs: 25 NAI (no action), 34 VAI (voluntary action), 4 OAI (official action). Leading inspection & GMP sites: United States (54), UNITED KINGDOM (52), Austria (51), Denmark (35), Germany (20).

Last updated 2026-08-22. Sourced from FDA, EMA EudraGMDP, MHRA GMDP, and ClinicalTrials.gov.

# CDMO Signal Score Quality FDA · GMP Capacity Programs
1
Novartis
Basel, Switzerland
88.3 90.9 15 insp · 62 GMP 135 programs
2
TF
Thermo Fisher Scientific
Plainville, MA · Alachua, FL · Cambridge, MA
83.1 97.9 6 insp · 10 GMP Available 2 programs
3
AG
AGC Biologics
Longmont, CO · Milan, IT · Copenhagen, DK · Chiba, JP
80.6 99.9 2 insp · 23 GMP Available 2 programs
4
TK
Takeda
Boston, MA · Zurich, CH
80.5 99.3 4 insp · 18 GMP 100 programs
5
Lonza
Basel, Switzerland
78.2 95.1 2 insp · 8 GMP 1 programs
6
OX
Oxford Biomedica
Oxford, United Kingdom
77.1 100.0 0 insp · 13 GMP Available 7 programs
7
CI
Cincinnati Children's Vector Production Facility
Cincinnati, OH
75.2 100.0 1 insp · 0 GMP 1 programs
8
NR
National Resilience
San Diego, CA · Boston, MA · RTP, NC · Philadelphia, PA
73.4 97.7 1 insp · 0 GMP Available 9 programs
9
CR
Charles River Laboratories
Newbury Park, CA · Memphis, TN · Keele, UK · Rockville, MD
91.7 98.7 8 insp · 11 GMP Limited 0 programs
10
RP
ReciBioPharm
Keele, UK · Sodertalje, SE
88.0 100.0 0 insp · 3 GMP 0 programs
11
PB
Pharmaron Biologics
San Diego, CA · Shaoxing, China, Liverpool, UK, Ningbo China
86.9 100.0 3 insp · 0 GMP Available 0 programs
12
AJ
Ajinomoto Bio-Pharma Services
San Diego, CA · Osaka, JP
85.6 100.0 0 insp · 1 GMP 0 programs
13
LB
Lotte Biologics
Incheon, KR · Syracuse, NY
83.7 100.0 1 insp · 0 GMP 0 programs
14
WB2
WuXi Biologics
Shanghai, CN · Wuxi, CN
83.7 100.0 0 insp · 4 GMP 0 programs
15
KB
KBI Biopharma
Durham, NC · Boulder, CO
83.5 100.0 1 insp · 1 GMP Limited 0 programs
16
FD
FUJIFILM Diosynth Biotechnologies
Research Triangle, NC · Holly Springs, NC · Hillerod, DK
83.5 100.0 0 insp · 23 GMP Expanding 0 programs
17
DH
Danaher (CGT Portfolio)
Washington, DC
81.5 0 programs
18
BR
BioReliance (Merck)
Glasgow, UK · Rockville, MD
81.0 98.8 4 insp · 8 GMP 0 programs
19
NW
Northway Biotech
Vilnius, LT; Waltham (MA), USA
80.8 100.0 0 insp · 8 GMP Available 0 programs
20
OB
OmniaBio
Hamilton, ON
79.5 100.0 0 insp · 2 GMP 0 programs
21
SK
SK pharmteco
Dublin, Ireland. Rancho Cordova, CA. King of Prussia, PA. Houston, TX. Korea. France.
79.5 100.0 Available 0 programs
22
PG
ProBioGen
Berlin, DE
78.9 100.0 0 insp · 2 GMP 0 programs
23
XP
eXmoor Pharma
Bristol, United Kingdom
78.7 100.0 0 insp · 1 GMP 0 programs
24
BB
bluebird bio Manufacturing
Durham, NC
78.5 0 programs
25
AA
Ascend Advanced Therapies
London, United Kingdom
78.1 100.0 0 insp · 1 GMP 0 programs
26
NG
NecstGen
Leiden, NL
78.1 100.0 0 insp · 1 GMP 0 programs
27
ET
Exothera
Jumet, BE
78.1 100.0 0 insp · 4 GMP 0 programs
28
CE
Celonic
Basel, Switzerland
78.1 100.0 0 insp · 1 GMP 0 programs
29
AD
Advent Bioservices
London, United Kingdom
78.1 100.0 0 insp · 2 GMP 0 programs
30
BV
Biovian
Turku, Finland
78.0 99.7 1 insp · 4 GMP 0 programs
31
AG2
August Bioservices
San Carlos, CA
77.4 98.5 1 insp · 0 GMP 0 programs
32
VG
Viralgen Vector Core
San Sebastián, Spain
76.8 100.0 0 insp · 4 GMP Available 0 programs
33
Catalent
Bagsværd, Denmark (operating under Novo Holdings; legacy US operations headquartered in Somerset, NJ)
76.5 79.3 12 insp · 35 GMP 0 programs
34
CA
Catalent (Novo Holdings)
Harmans, MD · Gosselies, BE
75.1 79.3 1 insp · 0 GMP Available 0 programs
35
IU
Indiana University Vector Production Facility
Indianapolis, IN
66.2 49 programs
How we score CDMOs →

What to evaluate in a Gene Therapy CDMO

Vector platform match
The first shortlist filter for any gene therapy program is vector platform. AAV for in vivo systemic; lentiviral for ex vivo cell engineering; adenoviral for vaccines and select high-expression programs. Filter by platform first, then compare within the platform.
Regulatory record on-platform
A CDMO with a strong FDA record on AAV manufacturing doesn't automatically de-risk lentiviral work — inspections are facility- and process-specific. Verify the inspection record on the exact platform and site your program will use.
Capacity match to phase
Early clinical AAV runs at 50-200L; commercial can reach 1000-2000L single-batch. Lentiviral commercial supply is a much narrower field. Confirm the CDMO's capacity headroom at your target phase before shortlisting.
Analytics maturity
Vector analytics — capsid ratio, titer, potency, RCL for lentivirus — drive lot release. A CDMO with qualified, established assays de-risks comparability and tech transfer.

Gene Therapy CDMOs — Frequently Asked Questions

Who are the top Gene Therapy CDMOs?
By CDMO Signal's independent Signal Score, the top-ranked Gene Therapy CDMOs include Novartis, Thermo Fisher Scientific, AGC Biologics. See the full ranked table above — scored on FDA, clinical, financial, and capacity data.
How many Gene Therapy CDMOs have FDA inspection records?
CDMO Signal tracks 16 Gene Therapy CDMOs with FDA inspection records and 250 EMA/MHRA GMP certificates across the group.
What should I look for in a gene therapy CDMO?
Match the vector platform to your program first (AAV / lentiviral / adenoviral). Then verify the CDMO's on-platform inspection record, capacity at your target phase, analytics maturity for that vector type, and a clean FDA and EMA/MHRA record. The individual platform pages have platform-specific detail.
How many gene therapy CDMOs does CDMO Signal track?
63 CDMOs are tracked as gene therapy manufacturers — the union of AAV, lentiviral, adenoviral, and generally-tagged gene therapy CDMOs. Each is scored independently on the standard four-pillar Signal Score composite.
Related modalities
AAV / Gene Therapy CDMOs Lentiviral Vector CDMOs Adenoviral Vector CDMOs Cell Therapy CDMOs
Other Modalities
AAV CAR-T Lentiviral Cell Therapy mRNA/LNP Plasmid DNA Biologics Oligo/ASO Adenoviral Gene Editing Exosome Recombinant Proteins ADC Cell & Gene Therapy