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Vaccines CDMO Companies
Vaccines Contract Manufacturing Services

Your Trusted Partners for Vaccines Contract Manufacturing and Development

Showing 18 facilities
HIPRA BIOTECH SERVICES | Amer
Spain

HIPRA BIOTECH SERVICES | Amer

HIPRA Biotech Services

End-to-end internal capabilities from cell line development to commercial manufacturing.

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

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

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

BSL (Biological Safety Level): 1, 2

USE: Human, Veterinary

BATCH SIZE: Large, Small, Medium

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

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, BIOLOGICS

REGION: Europe

JAFRAL
Slovenia

JAFRAL

JAFRAL

Integrated biotechnology facility providing R&D, non-GMP and GMP manufacturing, QC testing, and fill & finish services for advanced biologics.

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

COMPLIANCE: ICH, FDA (cGMP), ISO, EMA (EU GMP), World Health Organization (GMP / HACCP), SQF (Safe Quality Food)

MARKETS: EMA (EU), PMDA (Japan), FDA (USA), Health Canada (Canada), ANVISA (Brazil), MHRA (UK), SFDA (Saudi Arabia), Turkish Health Authorities, EDE (UAE), CDSCO (India), TGA (Australia)

BSL (Biological Safety Level): 1, 2

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

USE: Human, Veterinary

BATCH SIZE: Large, Small, Medium

CONTROLLED SUBSTANCES: Lowest potential for abuse

THERAPEUTIC AREAS OF EXPERTISE (ATC): (J) Antiinfectives for systemic use, (D) Dermatologicals, (V06) Nutrients, (R) Respiratory system, (A) Digestive tract and metabolism

REGION: Europe

Bilthoven Biologicals Drug Substance and Drug Product Facilities
Netherlands

Bilthoven Biologicals Drug Substance and Drug Product Facilities

Bilthoven Biologicals BV

Multi-product GMP facilities for Drug Substance and Drug Product.

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

MARKETS: EMA (EU), MHRA (UK)

BSL (Biological Safety Level): 1, 2

USE: Human

BATCH SIZE: Large, Small, Medium

COMPLIANCE: EMA (EU GMP)

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

REGION: Europe

53Biologics Production Plant
Spain

53Biologics Production Plant

53Biologics

53Biologics is a Spanish CDMO specialized in decoding the production of biologicals, from DNA to proteins.

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

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

REGION: Europe

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

BATCH SIZE: Large, Small, Medium

USE: Human, Veterinary

BSL (Biological Safety Level): 1, 2

CATEGORY / PRODUCT: BIOLOGICS

Cultiply
Spain

Cultiply

Cultiply

Spanish CDMO that develops production and purification processes for recombinant proteins, enzymes, DNA and other bioderived products.

MARKETS: EMA (EU), PMDA (Japan), NMPA (China), FDA (USA), Health Canada (Canada), ANVISA (Brazil), ISP (Chile), MSPAS (Guatemala), COFEPRIS (Mexico), DIGEMID (Peru), Russian Health Authorities, MHRA (UK), ANMAT (Argentina), INVIMA (Colombia), MFDS (South Korea), CDSCO (India), TGA (Australia)

REGION: Europe

COMPLIANCE: ISO

BSL (Biological Safety Level): 1, 2

SERVICES: Development services, Manufacturing services

CONTROLLED SUBSTANCES: Lowest potential for abuse

BATCH SIZE: Small, Medium

CATEGORY / PRODUCT: BIOLOGICS

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

Rodon Biologics
Portugal

Rodon Biologics

Rodon Biologics - RDN Serviços de Biotecnologia

Rodon Biologics provides excellence in the development of biopharmaceutical products for third parties.

REGION: Europe

CATEGORY / PRODUCT: NUTRACEUTICALS, BIOLOGICS, SERVICES

BSL (Biological Safety Level): 1, 2

SERVICES: Development services, Analytical / QC services

BATCH SIZE: Small

HIPRA BIOTECH SERVICES | Aiguaviva
Spain

HIPRA BIOTECH SERVICES | Aiguaviva

HIPRA Biotech Services

End-to-end internal capabilities from cell line development to commercial manufacturing.

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

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

REGION: Europe

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

BATCH SIZE: Large, Small, Medium

USE: Human

BSL (Biological Safety Level): 1, 2

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

CATEGORY / PRODUCT: BIOLOGICS

CZ Vaccines | Large Scale Plant Portugal
Portugal

CZ Vaccines | Large Scale Plant Portugal

CZ Vaccines

Commercial Scale Facility

MARKETS: EMA (EU)

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

REGION: Europe

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

BATCH SIZE: Large, Medium

USE: Human

BSL (Biological Safety Level): 1, 2

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

CATEGORY / PRODUCT: BIOLOGICS, FDF / DRUG PRODUCTS

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

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

REGION: Europe

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

USE: Human

BSL (Biological Safety Level): 1, 2

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

BATCH SIZE: Small

CATEGORY / PRODUCT: BIOLOGICS, FDF / DRUG PRODUCTS

CZ Vaccines | Large Scale Plant Spain
Spain

CZ Vaccines | Large Scale Plant Spain

CZ Vaccines

Single Use Commercial Scale Facility

MARKETS: EMA (EU)

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

REGION: Europe

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

BATCH SIZE: Large, Medium

USE: Human

BSL (Biological Safety Level): 1, 2

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

CATEGORY / PRODUCT: BIOLOGICS, FDF / DRUG PRODUCTS

Limited view

BIOLOGICS manufacturing site

MAI network supplier

Contract Development and Manufacturing Organization (CDMO) with a focus on recombinant proteins and monoclonal antibodies (mAbs).

Location available after registration

Limited view

COSMETICS manufacturing site

MAI network supplier

Creative Biostructure was founded with a strong focus on structural biology and membrane protein research.

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.