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Vaccines CDMO Companies
Vaccines Contract Manufacturing Services

Your Trusted Partners for Vaccines Contract Manufacturing and Development

Showing 18 facilities

BATCH SIZE: Small

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

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, BIOLOGICS, CHEMICAL-SYNTHETIC

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): 2

HIPRA BIOTECH SERVICES | Amer
Spain

HIPRA BIOTECH SERVICES | Amer

HIPRA Biotech Services

Capacidades internas integrales, desde el desarrollo de líneas celulares hasta la fabricación comercial

MARKETS: DIGEMID (Peru), ANMAT (Argentina), ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), EMA (EU), COFEPRIS (Mexico), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)

BATCH SIZE: Small, Medium, Large

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, SERVICES, OLIGONUCLEOTIDES, BIOLOGICS, CHEMICAL-SYNTHETIC

COMPLIANCE: ISP (Chile BPM), ANMAT (Argentina nueva GMP), EMA (EU GMP), PMDA/MHLW (Japan GMP), DIGEMID, ANVISA (Brazil B-GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), FDA (cGMP), ISO, INVIMA, Health Canada (Canada GMP), MSPAS, COFEPRIS

REGION: Europe

USE: Human, Veterinary

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

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 5,000 µg/day), 1 / low-hazard (PDE > 5,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)

BSL (Biological Safety Level): 1, 2

THERAPEUTIC AREAS OF EXPERTISE (ATC): (L) Antineoplastic and immunomodulating agents

HIPRA BIOTECH SERVICES | Aiguaviva
Spain

HIPRA BIOTECH SERVICES | Aiguaviva

HIPRA Biotech Services

Capacidades internas de principio a fin, desde el desarrollo de líneas celulares hasta la fabricación comercial.

MARKETS: DIGEMID (Peru), ANMAT (Argentina), ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), EMA (EU), COFEPRIS (Mexico), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)

BATCH SIZE: Small, Medium, Large

COMPLIANCE: ISP (Chile BPM), ANMAT (Argentina nueva GMP), EMA (EU GMP), PMDA/MHLW (Japan GMP), DIGEMID, ANVISA (Brazil B-GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), FDA (cGMP), ISO, INVIMA, Health Canada (Canada GMP), MSPAS, COFEPRIS

CATEGORY / PRODUCT: SERVICES, OLIGONUCLEOTIDES, BIOLOGICS, CHEMICAL-SYNTHETIC

REGION: Europe

USE: Human, Veterinary

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

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 5,000 µg/day), 1 / low-hazard (PDE > 5,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)

BSL (Biological Safety Level): 1, 2

THERAPEUTIC AREAS OF EXPERTISE (ATC): (L) Antineoplastic and immunomodulating agents

53Biologics Production Plant
Spain

53Biologics Production Plant

53Biologics

53Biologics es una CDMO espa ola especializada en descifrar la producción de biológicos, desde el ADN hasta las proteínas, proporcionando desde la fase preclíni

MARKETS: DIGEMID (Peru), ANMAT (Argentina), ANVISA (Brazil), ISP (Chile), FDA (USA), MSPAS (Guatemala), EMA (EU), COFEPRIS (Mexico), TGA (Australia), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)

BATCH SIZE: Small, Medium, Large

COMPLIANCE: EMA (EU GMP), World Health Organization (GMP / HACCP), FDA (cGMP), ISO

CATEGORY / PRODUCT: SERVICES, OLIGONUCLEOTIDES, BIOLOGICS, CHEMICAL-SYNTHETIC

REGION: Europe

USE: Human, Veterinary

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

BSL (Biological Safety Level): 1, 2

THERAPEUTIC AREAS OF EXPERTISE (ATC): (L) Antineoplastic and immunomodulating agents

Adragos Pharma | Jura
Switzerland

Adragos Pharma | Jura

Adragos Pharma

Nos especializamos en la fabricación aséptica de productos farmacéuticos y biofarmacéuticos estériles, liofilizados o líquidos, mediante procesos de llenado y a

BATCH SIZE: Small, Medium

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, SERVICES, BIOLOGICS, CHEMICAL-SYNTHETIC

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

REGION: Europe

USE: Human

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

MARKETS: PMDA (Japan), FDA (USA), EMA (EU), MFDS (South Korea), NMPA (China), Health Canada (Canada), MHRA (UK)

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 5,000 µg/day), 1 / low-hazard (PDE > 5,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)

CONTROLLED SUBSTANCES: High potential for abuse & no medical use

THERAPEUTIC AREAS OF EXPERTISE (ATC): (L) Antineoplastic and immunomodulating agents

CZ Vaccines | Large Scale Plant Portugal
Spain

CZ Vaccines | Large Scale Plant Portugal

CZ Vaccines

Instalación a Escala Comercial

BATCH SIZE: Medium, Large

THERAPEUTIC AREAS OF EXPERTISE (ATC): (R) Respiratory system, (L) Antineoplastic and immunomodulating agents, (G) Genito urinary system and sex hormones, (J) Antiinfectives for systemic use

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, BIOLOGICS, CHEMICAL-SYNTHETIC

COMPLIANCE: EMA (EU GMP), World Health Organization (GMP / HACCP), ISO

REGION: Europe

USE: Human

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

BSL (Biological Safety Level): 1, 2

MARKETS: EMA (EU)

CZ Vaccines | Large Scale Plant Spain
Spain

CZ Vaccines | Large Scale Plant Spain

CZ Vaccines

Instalación Comercial de Escala Comercial de Uso Único

BATCH SIZE: Medium, Large

THERAPEUTIC AREAS OF EXPERTISE (ATC): (R) Respiratory system, (M) Musculoskeletal system, (G) Genito urinary system and sex hormones, (J) Antiinfectives for systemic use, (N) Nervous system

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, OLIGONUCLEOTIDES, PARTICLE ENGINEERING, BIOLOGICS, CHEMICAL-SYNTHETIC

COMPLIANCE: EMA (EU GMP), World Health Organization (GMP / HACCP), ISO

REGION: Europe

USE: Human

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

BSL (Biological Safety Level): 1, 2

MARKETS: EMA (EU)

Rodon Biologics
Spain

Rodon Biologics

Rodon Biologics - RDN Serviços de Biotecnologia

Rodon Biologics ofrece excelencia en el desarrollo de productos biofarmacéuticos para terceros.

BATCH SIZE: Small

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, SERVICES, OLIGONUCLEOTIDES, BIOLOGICS, NUTRACEUTICALS, CHEMICAL-SYNTHETIC

REGION: Europe

USE: Human

SERVICES: Analytical / QC services, Manufacturing services, Development services

BSL (Biological Safety Level): 1, 2

THERAPEUTIC AREAS OF EXPERTISE (ATC): (L) Antineoplastic and immunomodulating agents

Limited view

FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

Organización de Desarrollo y Fabricación por Contrato (CDMO) con enfoque en proteínas recombinantes y anticuerpos monoclonales (mAbs).

Location available after registration

Limited view

FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

Instalaciones GMP multiproducto para sustancia activa y producto farmacéutico.

Location available after registration

Limited view

FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

Demo facility

Location available after registration

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As vaccine technologies evolve — from traditional attenuated viruses to recombinant proteins and mRNA platforms — the role of experienced vaccines CDMO companies has never been more critical. These specialized contract development and manufacturing organizations provide the infrastructure, technical expertise, and regulatory knowledge required to bring vaccines from concept to commercial production.

Whether you’re a biotech developing a novel prophylactic or a pharmaceutical company scaling up a therapeutic vaccine, working with trusted vaccines contract manufacturing partners ensures speed, safety, and scalability.


How to Choose Vaccines CDMO Companies

Choosing the right vaccines CDMO is essential for successful development, scale-up, and regulatory approval. Key factors to evaluate include:

  • Platform experience: Proven capabilities in live-attenuated, inactivated, subunit, viral vector, or mRNA vaccine platforms.
  • Process development expertise: Strong support for upstream (cell culture, fermentation) and downstream (purification, formulation) workflows.
  • Fill-finish capabilities: Sterile vialing or prefilled syringes in compliance with GMP standards.
  • Regulatory readiness: Experience with FDA, EMA, WHO PQ, and global health agency approvals.
  • Cold chain management: Support for ultra-low temperature storage and distribution.
  • Clinical to commercial scalability: Capacity to transition smoothly through development phases.

Working with a CDMO that aligns with your platform and regulatory path greatly reduces time and risk.


Key Services Offered by Vaccines Contract Manufacturers

Top-tier vaccines contract manufacturing providers typically offer:

  • Cell line and virus seed development
  • Upstream production: Using Vero, CHO, HEK293, or E. coli systems.
  • Purification and inactivation processes tailored to vaccine modality.
  • mRNA synthesis and LNP formulation
  • Sterile fill-finish, visual inspection, and labeling.
  • Analytical development and QC testing: Potency, endotoxins, sterility.
  • GMP manufacturing: For clinical trial material and commercial launch.
  • Global regulatory support and dossier preparation.

These services support the full lifecycle of vaccine development, from early research through global distribution.


Advantages of Partnering with Vaccines CDMO Companies

Choosing specialized vaccines CDMO companies provides measurable benefits:

  • Platform versatility: Across viral, bacterial, recombinant, and nucleic acid vaccines.
  • Faster time to clinic: Through integrated development and manufacturing processes.
  • Access to proprietary technologies: Such as adjuvants or nanoparticle delivery.
  • Strong regulatory track record: With approvals in major markets.
  • Reliable global supply chain: And cold chain infrastructure.

These CDMOs serve as strategic partners — not just manufacturers — enabling innovation and global access.


Vaccines CDMO Companies

  • 53Biologics: CDMO specialized in biologics production from DNA to proteins, providing preclinical to cGMP manufacturing. [See CDMO profile]
  • Mabion: Fully integrated CDMO offering development and GMP manufacturing of biotherapeutics, including monoclonal antibodies and recombinant proteins. [See CDMO profile]
  • Shilpa Biologicals: Supports process development, gene to cell line development, GMP manufacturing, formulation development, analytical development, fill-finish, and packaging. [See CDMO profile]
  • HIPRA BIOTECH SERVICES: End-to-end capabilities from cell line development to commercial manufacturing. [See CDMO profile]
  • Cultiply: Spanish CDMO developing production and purification processes for recombinant proteins, enzymes, DNA, and other bioderived products. [See CDMO profile]
  • Rodon Biologics: Provides development of biopharmaceutical products, antibodies, peptides, proteins, and hormones for third parties. [See CDMO profile]
  • CZ Vaccines: Single-use commercial scale facility. [See CDMO profile]
  • Adragos Pharma: Specializes in aseptic manufacturing of lyophilized or liquid sterile biopharmaceuticals through fill-and-finish. [See CDMO profile]
  • Demo facility: Tissue therapy, Cell therapy and GTMP (Gene Therapy). [See CDMO profile]
  • Bilthoven Biologicals Drug Substance and Drug Product Facilities: Multi-product GMP facilities for Drug Substance and Drug Product. [See CDMO profile]

Related Information


Let MAI CDMO Network Help You Find the Right Vaccines CDMO Partner

At MAI CDMO Network, we connect companies with the most capable vaccines CDMO companies worldwide — whether you’re producing a next-gen mRNA vaccine or scaling a live-attenuated product. Our network of vaccines contract manufacturing partners is built to help you meet development timelines, quality requirements, and regulatory expectations with confidence.

Need a reliable vaccine manufacturing partner? Contact us today to find the right fit for your platform and pipeline.