Category and country

CDMO companies in Finland

6 cdmo profiles in Finland. Every profile is hand-reviewed with leadership, certifications, and public sources.

Profiles6
Verified6
With certifications5
Cities4
Category view

Where does cdmo cluster in Finland?

Kuopio (2), Oulu (2), Helsinki (1), and Turku (1) Most visible profiles: Kuopio Center for Gene and Cell Therapy, Pharmatory, Paras Biopharmaceuticals Finland, and FinVector.

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Which standards are already visible?

GMP (5) and FDA-Inspected (2) Latest review: 24 April 2026. Review cycle: April 2026.

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CDMO profiles in Finland

6 profiles match the active filter.

Current review cycle

Kuopio Center for Gene and Cell Therapy

KuopioFinlandCDMO

Kuopio ATMP CDMO providing Fimea-authorized GMP viral-vector manufacturing (AAV, adenovirus, lentivirus) for gene and cell therapy programs, owned by Ferring Ventures since 2020.

Lead
Tuija KekarainenScientific Director and Cell Therapy Unit Director
Scale
GMP viral-vector manufacturing
0 sources38d reviewGMP Fimea-inspected manufacturer's authorizationATMP CDMO for gene and cell therapy
Current review cycle

Pharmatory

OuluFinlandCDMO

Oulu API CDMO providing process R&D, analytical services, and cGMP contract manufacturing for human and veterinary pharmaceutical clients.

Lead
Jaana KarjalainenCEO and Managing Director
Scale
Commercial and development-stage API platform
0 sources71d reviewOfficial leadership disclosureOfficial Oulu facility disclosurecGMP and EMA audit disclosure
Current review cycle

Paras Biopharmaceuticals Finland

OuluFinlandCDMO

Oulu biopharmaceutical company focused on biosimilars, recombinant biologics, and process technologies from a Finnish operating base.

Lead
Ashesh KumarFounder and Director
Scale
Development-stage biologics platform
0 sources71d reviewOfficial Oulu address disclosureOfficial leadership contact disclosureBiologics platform claim
Current review cycle

FinVector

KuopioFinlandCDMO

Kuopio gene-therapy CDMO and viral-products manufacturer operating cGMP production, drug-substance and drug-product suites, and a growing pharma campus in Savilahti.

Lead
Matthias KriegerManaging Director
Scale
Clinical-to-commercial gene-therapy manufacturing
0 sources72d reviewcGMP manufacturingFDA-approved drug manufacturer
Current review cycle

3PBIOVIAN

TurkuFinlandCDMO

Turku biologics and viral-vector CDMO site offering microbial proteins, plasmid DNA, viral vectors, aseptic fill-finish, and QC services under EMA-certified and FDA-inspected GMP operations.

Lead
Damaso MoleroChief Executive Officer
Scale
Investigational to commercial GMP manufacturing
0 sources72d reviewEMA-certified GMP productionFDA-inspected GMP manufacturing
Current review cycle

Nanoform Finland

HelsinkiFinlandCDMO

Helsinki particle-engineering CDMO using proprietary nanoforming technology to improve drug solubility and move small-molecule programs from development into clinical and commercial supply.

Lead
Edward HaeggstromChief Executive Officer
Scale
Clinical to Commercial
Related brief

Read deeper on this category

Market brief

European CDMO Capacity 2026: Biologics, Fill-Finish, Small Molecule

Where to look for biologics, fill-finish, small-molecule, and specialised CDMO capacity across Europe in 2026 — 33 CDMOs in the directory across 9 countries, organised by what they actually do and where they sit.

Open brief
FAQ

Frequently asked questions on this category

What is a CDMO?
A Contract Development and Manufacturing Organization handles drug development and production for other pharma or biotech companies. The work spans process development, scale-up, GMP manufacturing, fill-finish, packaging, and analytical testing.
Which European countries have the most CDMO capacity?
Switzerland and Germany lead by depth and quality (Basel, Heidelberg, Mainz). Poland adds large-scale manufacturing capacity, Lithuania has a growing biologics CDMO presence anchored in Vilnius, and the Nordics carry strong fill-finish and aseptic operators in Denmark and Sweden.
How are these CDMO companies verified?
Every profile is hand-reviewed against an audit framework: leadership identity 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 the company's current operating context.
Can I compare two CDMO providers side by side?
Yes — use the Compare button on any company card to add it to a comparison set (up to 3 companies), then open the /compare page for a side-by-side view of leadership, certifications, and operating scale.
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