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NDC CDMO Companies
Nanobody-drug Conjugate Contract Manufacturing Services

Your Trusted Partners for Nanobody-drug Conjugate Contract Manufacturing and Development

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FDF / DRUG PRODUCTS manufacturing site

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Bioconjugados (ADC) y fabricación clínica y comercial de anticuerpos

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FDF / DRUG PRODUCTS manufacturing site

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Demo facility

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FDF / DRUG PRODUCTS manufacturing site

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Soluciones integrales de CDMO para API e intermedios clave.

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These facilities match your main criteria but not every optional filter — including other countries in the same region.

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

CARBOGEN AMCIS | Bubendorf
Switzerland

CARBOGEN AMCIS | Bubendorf

CARBOGEN AMCIS

Desarrollo y fabricación cGMP de API de gran potencia, incluidos conjugados anticuerpo-fármaco (ADC)

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

BATCH SIZE: Small, Medium

THERAPEUTIC AREAS OF EXPERTISE (ATC): (R) Respiratory system, (V09-10) Radiopharmaceuticals, (M) Musculoskeletal system, (L) Antineoplastic and immunomodulating agents, (C) Cardiovascular system, (A) Digestive tract and metabolism, (D) Dermatologicals, (N) Nervous system, (B) Blood and blood forming organs

COMPLIANCE: EMA (EU GMP), PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), World Health Organization (GMP / HACCP), FDA (cGMP), ISO

CATEGORY / PRODUCT: SERVICES, BIOLOGICS, CHEMICAL-SYNTHETIC

REGION: Europe

USE: Human, Veterinary

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

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 5,000 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 1 / low-hazard (PDE > 5,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)

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COSMETICS manufacturing site

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Planta de fermentación

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SERVICES manufacturing site

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CDMO espa ola que desarrolla procesos de producción y purificación de proteínas recombinantes, enzimas, ADN y otros productos bioderivados.

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FDF / DRUG PRODUCTS manufacturing site

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Desarrollo y fabricación de medicamentos en formas sólidas orales (OSD), nasales, inhaladas y polvos y líquidos estériles.

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SERVICES manufacturing site

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Mabion es una CDMO totalmente integrada que ofrece una amplia gama de servicios relacionados con el desarrollo y la fabricación GMP de bioterapéuticos, incluidos anticuerpos monoclonales y cualquier…

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SERVICES manufacturing site

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Su socio CDMO de confianza, con más de 30 a os de experiencia en el desarrollo y la fabricación de biofármacos, vectores virales y vacunas.

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SERVICES manufacturing site

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Biopharma Contract Packaging

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Nanobody-drug conjugates (NDCs) are gaining momentum as next-generation targeted therapies, offering improved tissue penetration and faster clearance compared to traditional antibodies. These novel biologics demand a unique combination of biologics, chemistry, and conjugation expertise — making specialized NDC CDMO companies essential partners in their development.

As an evolution of ADCs, NDCs present specific formulation, scalability, and regulatory challenges. Collaborating with experts in nanobody-drug conjugate contract manufacturing ensures the necessary infrastructure, compliance, and technical know-how are in place to move from discovery through clinical and commercial production.


How to Choose NDC CDMO Companies

When selecting among NDC CDMO companies, it’s crucial to consider partners with experience in both biologics and HPAPIs, and who understand the specific demands of nanobody-based platforms. Key criteria include:

  • Nanobody engineering expertise: Including single-domain antibody expression systems.
  • Site-specific and stochastic conjugation capabilities.
  • Experience with linker-payload strategies: Tailored to smaller scaffold proteins.
  • HPAPI containment and GMP conjugation: Infrastructure for safe handling.
  • Custom analytics: For DAR, aggregation, and nanobody integrity.
  • Regulatory familiarity: With first-in-class and orphan nanobody therapeutics.

Not all ADC CDMOs are equipped for nanobody platforms — choosing one that is ensures a better technical and regulatory fit.


Key Services Offered by Nanobody-drug Conjugate Contract Manufacturers

Nanobody-drug conjugate contract manufacturing typically includes:

  • Nanobody production: Via microbial (E. coli, yeast) or mammalian expression systems.
  • Payload synthesis: And linker optimization for low molecular weight targets.
  • Conjugation development and scale-up: Under GMP conditions.
  • Analytical testing: DAR, SDS-PAGE, SEC, HPLC, and bioactivity assays.
  • Formulation and fill-finish: For parenteral delivery.
  • Stability studies and cold chain packaging.
  • CMC support: For IND and CTA submissions.

These tailored services ensure safety, precision, and manufacturability across nanobody-based therapeutics.


Advantages of Partnering with NDC CDMO Companies

Engaging specialized NDC CDMO companies provides distinct advantages:

  • Smaller-scale process optimization: Ideal for early-stage and orphan drugs.
  • Improved targeting: Of solid tumors and difficult-to-access tissues via nanobodies.
  • Integrated platforms: That combine biologics, chemistry, and GMP fill-finish.
  • Faster development timelines: With access to existing nanobody production know-how.
  • Compliance with biologics and HPAPI standards: For global submissions.

These CDMOs understand the structural and regulatory nuances of nanobody-drug conjugates and can adapt processes accordingly.


NDC CDMO Companies

Some of the leading NDC CDMO companies with emerging or established capabilities include:

  • 53Biologics: CDMO specialized in decoding biologics production, from DNA to proteins, providing services from preclinical to cGMP manufacturing. [See CDMO profile]
  • Shilpa Biologicals: CDMO supporting process development, from gene to cell line development to GMP, formulation development, analytical development, drug substance, drug product, fill-finish, and packaging. [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 CDMO solutions for Abs (antibodies), ADC & NDC (antibody-drug) manufacturing, API and key intermediates. [See CDMO profile]
  • CARBOGEN AMCIS: Development and cGMP manufacturing of highly potent APIs, including antibody-drug conjugates (ADC). [See CDMO profile]
  • Mabion: Fully integrated CDMO offering a wide range of services for the development and GMP manufacturing of biotherapeutics, including monoclonal antibodies and other recombinant protein-based products. [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 NDC CDMO Partner

At MAI CDMO Network, we specialize in connecting you with the most capable NDC CDMO companies to develop and manufacture your nanobody-drug conjugate efficiently and compliantly. From early-phase development to commercial production, our network of nanobody-drug conjugate contract manufacturing partners is ready to accelerate your program.

Let’s find your perfect fit. Contact us today to discover NDC CDMOs aligned with your molecule, modality, and timeline.