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Gene Therapy CDMO Companies
Viral Vector & Gene Therapy Manufacturing Services

Your Trusted CDMO Partners For Viral Vector Development, GMP Manufacturing & Gene Therapy Manufacturing Services

Showing 8 facilities
VIVEbiotech
Spain

VIVEbiotech

VIVEbiotech

Your leading GMP-certified CDMO exclusively dedicated to the production of lentiviral vectors.

BATCH SIZE: Small, Medium, Large

COMPLIANCE: EMA (EU GMP), MHRA (UK GMP), French Service-Public (CIR), FDA (cGMP)

REGION: Europe

USE: Human

SERVICES: Analytical / QC services, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services

MARKETS: FDA (USA), EMA (EU), MHRA (UK)

CATEGORY / PRODUCT: BIOLOGICS

BSL (Biological Safety Level): 1, 2

BATCH SIZE: Small

THERAPEUTIC AREAS OF EXPERTISE (ATC): (R) Respiratory system, (G) Genito urinary system and sex hormones, (A) Digestive tract and metabolism

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, BIOLOGICS

COMPLIANCE: EMA (EU GMP), ANVISA (Brazil B-GMP), World Health Organization (GMP / HACCP), ISO

REGION: Europe

MARKETS: ANVISA (Brazil), CDSCO (India), EMA (EU)

USE: Human

SERVICES: Analytical / QC services, Logistics, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services

BSL (Biological Safety Level): 1, 2

Cellex Cell Professionals
Germany

Cellex Cell Professionals

Cellex Cell Professionals

CGT CDMO Cell Manufacturing Plant and Collection Center for Starting Materials

BATCH SIZE: Small, Medium, Large

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, SERVICES, BIOLOGICS

COMPLIANCE: EMA (EU GMP), FDA (cGMP)

REGION: Europe

USE: Human, Veterinary

SERVICES: Analytical / QC services, Logistics, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services

MARKETS: FDA (USA), EMA (EU)

BSL (Biological Safety Level): 1, 2

Green Phoenix Labs GmbH
Germany

Green Phoenix Labs GmbH

Green Phoenix Labs GmbH

Cell Therapy company with excess Cleanroom capacity.

BATCH SIZE: Small, Medium

THERAPEUTIC AREAS OF EXPERTISE (ATC): (R) Respiratory system, (M) Musculoskeletal system, (G) Genito urinary system and sex hormones, (C) Cardiovascular system, (A) Digestive tract and metabolism, (D) Dermatologicals, (N) Nervous system, (B) Blood and blood forming organs

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, SERVICES, BIOLOGICS

COMPLIANCE: EMA (EU GMP)

CONTROLLED SUBSTANCES: Lowest potential for abuse, Lower potential for abuse, Low potential for abuse

REGION: Europe

USE: Human

SERVICES: Logistics, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)

BSL (Biological Safety Level): 1

MARKETS: EMA (EU)

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BIOLOGICS manufacturing site

MAI network supplier

Your trusted CDMO partner with experience in the development and manufacturing of biopharmaceuticals, viral vectors, and vaccines.

Location available after registration

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FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

mRNA & LNP manufacturing and Fill and Finish.

Location available after registration

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FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

Contract Development & Manufacturing Organisation

Location available after registration

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Gene therapies — including viral vector-based treatments, gene editing platforms, and advanced genetic medicines — require highly specialized manufacturing capabilities and strict GMP compliance. Biotech and pharmaceutical innovators rely on experienced gene therapy CDMO companies to support complex development workflows and scalable production of genetic medicines.

From early vector design through commercial-scale manufacturing, partnering with a specialized gene therapy contract manufacturing organization ensures product quality, regulatory readiness, and efficient technology transfer — key factors in successful gene therapy development.

How to Choose Gene Therapy CDMO Companies

Selecting the right gene therapy CDMO companies requires evaluating expertise in viral vector production, process scalability, and regulatory compliance. Important criteria include:

  • Viral vector expertise: AAV, lentiviral, adenoviral, and retroviral manufacturing platforms.
  • Plasmid DNA production capabilities: Critical for upstream gene therapy workflows.
  • Process development and scale-up: From research batches to commercial volumes.
  • Upstream and downstream processing: Cell culture systems, purification, and filtration technologies.
  • Analytical development: Vector characterization, potency assays, and genome integrity testing.
  • Regulatory expertise: FDA, EMA, and global gene therapy submissions and inspections.

A specialized CDMO ensures robust production systems and reliable manufacturing performance.

Key Services Offered by Gene Therapy Contract Manufacturers

Leading gene therapy contract manufacturing organizations typically provide:

  • Vector design and development: Optimization of gene delivery systems.
  • GMP viral vector manufacturing: Clinical and commercial production.
  • Plasmid DNA manufacturing: For research, clinical trials, and commercial use.
  • Process characterization: Upstream optimization and downstream purification.
  • Fill-finish services: Sterile filling for gene therapy products.
  • Analytical testing: Identity, purity, potency, and safety assays.
  • Tech transfer and scale-up: Transition from development to large-scale manufacturing.

These services help accelerate development timelines while maintaining quality and compliance.

Advantages of Partnering with Gene Therapy CDMO Companies

Working with specialized gene therapy CDMO companies offers multiple strategic benefits:

  • Access to specialized infrastructure: Viral vector manufacturing suites and biosafety facilities.
  • Accelerated clinical development: Through established manufacturing platforms.
  • Risk reduction: Using validated production and purification technologies.
  • Scalable production models: Supporting early clinical to commercial demand.
  • Regulatory confidence: Leveraging experienced quality and compliance teams.

An experienced CDMO enables efficient translation of gene therapy innovations into clinical and commercial products.

Gene Therapy CDMO Companies

Some of the most recognized gene therapy CDMO companies include:

  • VIVEbiotech: Your leading GMP-certified CDMO exclusively dedicated to the production of lentiviral vectors. [See CDMO profile]
  • CZ Vaccines: CDMO specialized in advanced biological products with capabilities supporting cell-based and innovative therapies. [See CDMO profile]
  • Cellex: CGT CDMO Cell Manufacturing Plant and Collection Center for Starting Materials. [See CDMO profile]
  • HiTech Health: Contract Development & Manufacturing Organisation. [See CDMO profile]
  • Northway Biotech: Global End-to-End Biologics CDMO. [See CDMO profile]
  • Green Phoenix Labs GmbH: Cell Therapy company with excess Cleanroom capacity. [See CDMO profile]
  • SyVento Biotech: mRNA & LNP manufacturing, F&F. [See CDMO profile]
  • HiTech Health: Contract Development & Manufacturing Organisation. [See CDMO profile]
  • ProBioGen: Your trusted CDMO partner with more than 30 years experience in the development and manufacturing of biopharmaceuticals, viral vectors, and vaccines. [See CDMO profile]

Related Information

Let MAI CDMO Help You Find the Right Gene Therapy CDMO Partner

At MAI CDMO, we connect biotech innovators with top-tier gene therapy CDMO companies offering viral vector development, plasmid DNA manufacturing, and GMP gene therapy production. Whether you require AAV manufacturing, lentiviral vector production, or full-scale commercial supply, our network ensures quality, compliance, and scalability.

Looking for a trusted gene therapy manufacturing partner? Contact us today to accelerate your gene therapy program.