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Recombinant Enzymes CDMO Companies
Enzymes Contract Manufacturing Services

Your Trusted Partners for Enzymes Contract Manufacturing and Development

Showing 24 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)

BDI biotech Production Plant
Spain

BDI biotech Production Plant

BDI biotech

Trabajamos como departamento de I+D especializado en el desarrollo de cepas y bioprocesos, el escalado y la producción de lotes.

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

CATEGORY / PRODUCT: SERVICES, BIOLOGICS, CHEMICAL-SYNTHETIC

REGION: Europe

USE: Human

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

COMPLIANCE: FDA (cGMP), ISO

BSL (Biological Safety Level): 1

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

SERVICES manufacturing site

MAI network supplier

Instalación de fabricación de biológicos conforme a GMP, especializada en enzimas y proteínas recombinantes para aplicaciones de fabricación biofarmacéutica y de péptidos.

Location available after registration

Limited view

FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

CDMO global de servicios integrales en biológicos

Location available after registration

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Recombinant enzymes are vital components in modern therapeutics, diagnostics, and industrial biotech. From rare disease enzyme replacement therapies (ERTs) to enzymes used in vaccine production, these biologics require highly specialized development and manufacturing processes. That’s why companies turn to expert recombinant enzymes CDMO companies to ensure efficiency, quality, and regulatory compliance.

Whether you’re developing a novel therapeutic enzyme or scaling a recombinant biocatalyst, partnering with the right enzymes contract manufacturing organization can reduce time to market and ensure product success at every stage.


How to Choose Recombinant Enzymes CDMO Companies

When evaluating recombinant enzymes CDMOs, keep these key criteria in mind:

  • Expression system flexibility: Can the CDMO work with microbial, yeast, or mammalian platforms?
  • Process development experience: Proven ability to optimize yields while maintaining bioactivity and stability.
  • Purification strategies: Expertise in isolating high-purity enzymes, including those prone to degradation.
  • Analytical capabilities: Robust testing for potency, structure, and contaminant clearance.
  • Scalability: Facilities that support seamless transition from R&D to GMP commercial production.
  • Regulatory track record: Familiarity with ERT, diagnostic, or food enzyme regulatory pathways (FDA, EMA, etc.).

Specialized enzyme CDMOs not only understand biologics — they understand enzymes specifically, from folding to function.


Key Services Offered by Enzymes Contract Manufacturers

Top-tier enzymes contract manufacturing organizations offer a wide array of services tailored to the needs of recombinant enzymes:

  • Strain and cell line development: Optimized for target enzyme expression.
  • Upstream development: Using microbial (E. coli, Pichia pastoris) or mammalian systems.
  • Downstream purification: Techniques like affinity, ion-exchange, and hydrophobic interaction chromatography.
  • Enzyme stabilization and formulation: For injectable or lyophilized formats.
  • Comprehensive analytical testing: Activity assays, purity, structure confirmation, endotoxin testing.
  • GMP manufacturing: For clinical and commercial use.
  • CMC documentation and global regulatory support.

Whether for medical, diagnostic, or industrial use, these services ensure consistent, compliant enzyme production.


Advantages of Partnering with Recombinant Enzymes CDMO Companies

Working with specialized recombinant enzymes CDMO companies brings unique advantages:

  • Therapeutic focus: Deep experience with enzymes as APIs in rare disease treatments or biologic support roles.
  • Optimized productivity: Proven approaches to maximize enzyme yield and minimize degradation.
  • Custom process design: For enzyme-specific folding, cofactor requirements, and stabilization.
  • Regulatory strength: From IND through commercial filings.
  • Speed to market: Via integrated development and manufacturing platforms.

These benefits are especially critical for companies working on high-complexity or low-volume enzyme programs.


Recombinant Enzymes CDMO Companies

Some of the most recognized recombinant enzymes CDMO companies include:

  • 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]
  • Cambrex Wiesbaden: Expertise in enzyme screening and development of over 800 proprietary enzymes. [See CDMO profile]
  • Cultiply: Spanish CDMO developing production and purification processes for recombinant proteins, enzymes, DNA, and other bioderived products. [See CDMO profile]
  • SINOWAY INDUSTRIAL CO: One-stop solutions for antibodies, ADCs, APIs, and key intermediates. [See CDMO profile]
  • Rodon Biologics: Development and manufacturing of antibodies, peptides, proteins, and hormones for third parties. [See CDMO profile]
  • CZ Vaccines: Single-use commercial scale biopharmaceutical manufacturing. [See CDMO profile]
  • BDI Biotech Production Plant: R&D focused on strain and bioprocess development, scale-up, and batch production. [See CDMO profile]
  • Adragos Pharma: Aseptic manufacturing of lyophilized or liquid sterile biopharmaceuticals via fill-and-finish operations. [See CDMO profile]
  • Kemwell Biopharma Pvt Ltd: Biologics-focused Contract Development and Manufacturing (CDMO) company providing development and manufacturing services to global biopharmaceutical organizations. [See CDMO profile]
  • Demo facility: Tissue therapy, Cell therapy and GTMP (Gene Therapy). [See CDMO profile]

Related Information


Let MAI CDMO Network Help You Find the Right Recombinant Enzymes CDMO Partner

At MAI CDMO Network, we specialize in identifying the best recombinant enzymes CDMO companies to support your product goals. Whether you’re scaling an enzyme replacement therapy or producing an enzyme for bioprocessing, we connect you with trusted enzymes contract manufacturing partners with the right technology, capacity, and regulatory expertise.

Need a manufacturing partner you can trust? Contact us today and let us match you with the ideal enzyme CDMO.