What is the difference between a manufacturer and a CDMO?

A manufacturer primarily produces its own drug substance, drug product, or device for its own pipeline or commercial supply. A CDMO (Contract Development and Manufacturing Organization) takes external programs from other companies — process transfer, scale-up, contract production. Some companies operate as both: manufacturing their own pipeline AND offering excess capacity to external clients.

Which European countries have the most manufacturing capacity?

Germany leads by industrial depth (Boehringer Ingelheim, Bayer, BioNTech production, Merck KGaA). Switzerland concentrates premium-tier sites (Roche, Novartis manufacturing). Denmark anchors aseptic/biologics scale (Novo Nordisk). Sweden adds AstraZeneca's Gothenburg base. Poland is competitive on cost (Polpharma, Adamed). Lithuania and Estonia have growing biologics manufacturing (Northway, Icosagen).

What certifications should a biotech manufacturer hold?

For drugs and biologics: GMP (essential, country-specific national authority enforces in EU). For medical devices: ISO 13485 + CE marking under MDR/IVDR. For US-bound supply: FDA inspection. For nonclinical studies: GLP. Use the /compliance pages on this directory to filter by specific markers — every published company has its certification context documented and source-backed.

How are manufacturers verified in this directory?

Every profile is hand-reviewed: leadership confirmed by primary source, physical site address sourced from official disclosures, regulatory matrix (GMP / ISO-13485 / GLP / FDA-Inspected) backed by certification documents, and a registry note explaining current operating context and production scope.

Category and country

Manufacturing companies in Denmark

4 manufacturing profiles in Denmark. Every profile is hand-reviewed with leadership, certifications, and public sources.

All Denmark biotech Manufacturing across Europe

Profiles4

Verified4

With certifications4

Cities4

Category view

Where does manufacturing cluster in Denmark?

Horsholm (1), Kalundborg (1), Kastrup (1), and Kvistgaard (1) Most visible profiles: Ferring Pharmaceuticals Denmark, ALK-Abelló, Bavarian Nordic, and Novo Nordisk Kalundborg.

Category view

Which standards are already visible?

GMP (4) Latest review: 22 March 2026. Review cycle: March 2026.

Full list

Manufacturing profiles in Denmark

4 profiles match the active filter.

Kastrup pharmaceutical operator within Ferring's global footprint, linking Denmark into fertility, maternal health, gastroenterology, and peptide-based pharmaceutical operations.

Lead: Tom PolaertsExecutive Vice President, Global Operations
Scale: Global pharma-operations footprint

Hørsholm allergy-immunotherapy headquarters and production-control node anchored in standardized vaccine manufacturing and quality systems.

Lead: Peter HallingPresident and Chief Executive Officer
Scale: Commercial specialty manufacturing

Kvistgaard vaccine-development and manufacturing anchor with commercial biodefense and travel-vaccine platforms operating inside a regulated global network.

Lead: Paul ChaplinPresident and Chief Executive Officer
Scale: Commercial vaccine manufacturing

Kalundborg is the flagship Danish industrial complex for API, biologics, and large-scale metabolic-disease manufacturing within Novo Nordisk's global network.

Lead: Lars Fruergaard JørgensenPresident and Chief Executive Officer
Scale: Global commercial manufacturing

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FAQ

Frequently asked questions on this category

What is the difference between a manufacturer and a CDMO?: A manufacturer primarily produces its own drug substance, drug product, or device for its own pipeline or commercial supply. A CDMO (Contract Development and Manufacturing Organization) takes external programs from other companies — process transfer, scale-up, contract production. Some companies operate as both: manufacturing their own pipeline AND offering excess capacity to external clients.
Which European countries have the most manufacturing capacity?: Germany leads by industrial depth (Boehringer Ingelheim, Bayer, BioNTech production, Merck KGaA). Switzerland concentrates premium-tier sites (Roche, Novartis manufacturing). Denmark anchors aseptic/biologics scale (Novo Nordisk). Sweden adds AstraZeneca's Gothenburg base. Poland is competitive on cost (Polpharma, Adamed). Lithuania and Estonia have growing biologics manufacturing (Northway, Icosagen).
What certifications should a biotech manufacturer hold?: For drugs and biologics: GMP (essential, country-specific national authority enforces in EU). For medical devices: ISO 13485 + CE marking under MDR/IVDR. For US-bound supply: FDA inspection. For nonclinical studies: GLP. Use the /compliance pages on this directory to filter by specific markers — every published company has its certification context documented and source-backed.
How are manufacturers verified in this directory?: Every profile is hand-reviewed: leadership confirmed by primary source, physical site address sourced from official disclosures, regulatory matrix (GMP / ISO-13485 / GLP / FDA-Inspected) backed by certification documents, and a registry note explaining current operating context and production scope.

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