Commercial-Scale AAV / Gene Therapy CDMOs

31
CDMOs tracked
31
Fully scored
14
With FDA records
39
FDA inspections
180
EMA/MHRA GMP certs
2
Warning letters

Adeno-associated virus (AAV) is the dominant delivery platform for in vivo gene therapy, from rare-disease programs to larger systemic indications. Rising demand has pushed CDMOs to scale suspension processes and tighten full/empty capsid analytics.

Selecting an AAV CDMO hinges on serotype experience, suspension vs adherent platform, full/empty capsid separation, and a proven regulatory record. The rankings below score each manufacturer on FDA inspections, GMP certification, clinical activity, and capacity.

FDA inspection outcomes across these CDMOs: 15 NAI (no action), 23 VAI (voluntary action), 1 OAI (official action). Leading inspection & GMP sites: UNITED KINGDOM (50), United States (36), Denmark (30), Germany (17), UNITED STATES (12).

Last updated 2026-06-29. Sourced from FDA, EMA EudraGMDP, MHRA GMDP, and ClinicalTrials.gov.

# CDMO Signal Score Quality FDA · GMP Capacity Programs
1
CR
Charles River Laboratories
Newbury Park, CA · Memphis, TN · Keele, UK · Rockville, MD
91.7 98.7 7 insp · 11 GMP Limited 0 programs
2
RP
ReciBioPharm
Keele, UK · Sodertalje, SE
88.0 100.0 0 insp · 3 GMP 0 programs
3
PB
Pharmaron Biologics
San Diego, CA · Shaoxing, CN
85.6 100.0 3 insp · 0 GMP 0 programs
4
AJ
Ajinomoto Bio-Pharma Services
San Diego, CA · Osaka, JP
85.6 100.0 0 insp · 1 GMP 0 programs
5
LB
Lotte Biologics
Incheon, KR · Syracuse, NY
83.7 100.0 1 insp · 0 GMP 0 programs
6
WB2
WuXi Biologics
Shanghai, CN · Wuxi, CN
83.7 100.0 0 insp · 4 GMP 0 programs
7
KB
KBI Biopharma
Durham, NC · Boulder, CO
83.5 100.0 1 insp · 1 GMP Limited 0 programs
8
FD
FUJIFILM Diosynth Biotechnologies
Research Triangle, NC · Holly Springs, NC · Hillerod, DK
83.5 100.0 0 insp · 18 GMP Expanding 0 programs
9
TF
Thermo Fisher Scientific
Plainville, MA · Alachua, FL · Cambridge, MA
83.1 97.9 5 insp · 10 GMP Available 2 programs
10
DH
Danaher (CGT Portfolio)
Washington, DC
81.5 0 programs
11
BR
BioReliance (Merck)
Glasgow, UK · Rockville, MD
81.0 98.8 2 insp · 8 GMP 0 programs
12
NW
Northway Biotech
Vilnius, LT; Waltham (MA), USA
80.8 100.0 0 insp · 8 GMP Available 0 programs
13
AG
AGC Biologics
Longmont, CO · Milan, IT · Copenhagen, DK · Chiba, JP
80.6 99.9 1 insp · 23 GMP Available 2 programs
14
TK
Takeda
Boston, MA · Zurich, CH
80.5 99.3 3 insp · 18 GMP 100 programs
15
OB
OmniaBio
Hamilton, ON
79.5 100.0 0 insp · 2 GMP 0 programs
16
PG
ProBioGen
Berlin, DE
78.9 100.0 0 insp · 2 GMP 0 programs
17
XP
eXmoor Pharma
Bristol, UK
78.7 100.0 0 insp · 1 GMP 0 programs
18
Lonza
Basel, Switzerland
78.2 95.1 2 insp · 8 GMP 1 programs
19
AA
Ascend Advanced Therapies
Philadelphia, PA
78.1 100.0 0 insp · 1 GMP 0 programs
20
NG
NecstGen
Leiden, NL
78.1 100.0 0 insp · 1 GMP 0 programs
21
ET
Exothera
Jumet, BE
78.1 100.0 0 insp · 4 GMP 0 programs
22
CE
Celonic
Basel, Switzerland
78.1 100.0 0 insp · 1 GMP 0 programs
23
AD
Advent Bioservices
London, UK
78.1 100.0 0 insp · 2 GMP 0 programs
24
BV
Biovian
Turku, Finland
78.0 99.7 1 insp · 4 GMP 0 programs
25
AG2
August Bioservices
San Carlos, CA
77.4 98.5 1 insp · 0 GMP 0 programs
26
OX
Oxford Biomedica
Oxford, United Kingdom
77.1 100.0 0 insp · 13 GMP Available 7 programs
27
VG
Viralgen Vector Core
San Sebastián, Spain
76.8 100.0 0 insp · 4 GMP Available 0 programs
28
Catalent
Somerset, NJ (now operating under Novo Holdings, HQ effectively Bagsværd, Denmark)
76.5 79.3 10 insp · 32 GMP 0 programs
29
CI
Cincinnati Children's Vector Production Facility
Cincinnati, OH
75.2 100.0 1 insp · 0 GMP 1 programs
30
CA
Catalent (Novo Holdings)
Harmans, MD · Gosselies, BE
75.1 79.3 1 insp · 0 GMP Available 0 programs
31
IU
Indiana University Vector Production Facility
Indianapolis, IN
66.2 46 programs
How we score CDMOs →

What to evaluate in a AAV / Gene Therapy CDMO

Platform & scale
Suspension processes scale better than adherent (HEK293) for commercial volumes. Confirm the CDMO's largest validated bioreactor scale and serotype track record.
Capsid quality
Full/empty capsid ratio and aggregate control drive potency and safety. Ask about AUC, anion-exchange separation, and the analytics package for capsid characterization.
Regulatory readiness
For programs heading to BLA, a strong FDA inspection history and EMA/MHRA GMP coverage matter — both are shown above and on each profile.
Capacity & timelines
AAV manufacturing slots can be constrained. Weigh the capacity signal and clinical-program load before committing.

AAV / Gene Therapy CDMOs — Frequently Asked Questions

Who are the top AAV / Gene Therapy CDMOs?
By CDMO Signal's independent Signal Score, the top-ranked AAV / Gene Therapy CDMOs include Charles River Laboratories, ReciBioPharm, Pharmaron Biologics. See the full ranked table above — scored on FDA, clinical, financial, and capacity data.
How many AAV / Gene Therapy CDMOs have FDA inspection records?
CDMO Signal tracks 14 AAV / Gene Therapy CDMOs with FDA inspection records and 180 EMA/MHRA GMP certificates across the group.
What should I look for in an AAV CDMO?
Look for serotype experience, a scalable suspension platform, strong full/empty capsid analytics, and a clean FDA and EMA/MHRA record. Match validated bioreactor scale to your dose and indication.
What's the difference between AAV and lentiviral CDMOs?
AAV is non-integrating and produced at higher volumes for in vivo gene therapy. Lentivirus integrates into the genome, is made under BSL-2 with RCL testing, and is used mainly for ex vivo cell engineering like CAR-T.
Related modalities
Lentiviral Vector CDMOs Gene Editing CDMOs Plasmid DNA CDMOs
Other Modalities
CAR-T Lentiviral Cell Therapy mRNA/LNP Plasmid DNA Biologics Oligo/ASO Adenoviral Gene Editing Exosome Recombinant Proteins ADC