Services / Nanomedicines

We know Nano™

One of Europe’s most advanced nanomedicine platforms. Lipid nanoparticles, polymeric nanoparticles, liposomes, nanosuspensions – and the complex delivery systems now reaching clinical development. Purpose-built GMP Annex 1 facility. Scientists who have been doing this for decades. Few CDMOs in Europe know nanomedicine like we do.

Our Expertise

Guiding Your Nanomedicine Candidate to the Clinic

Four nanoparticle platforms. One integrated team. The depth of expertise your molecule needs.

Ardena is a nanomedicine CDMO working across lipid nanoparticles, polymeric nanoparticles, metal nanoparticles and drug conjugates (ADCs and XDCs). One team carries a program from precursor manufacturing, through GMP manufacturing and fill and finish, to the regulatory file.

Our Facility

Nanomedicine Facility

Ardena has expanded its capabilities with a new 2,200 m² nanomedicine facility at Pivot Park.

Exterior of an Ardena facility building displaying the Ardena logo against a blue sky
Oss, Netherlands

Ardena Oss

Oss, Netherlands 160+ employees

Ardena has expanded its capabilities with a new 2,200 m² nanomedicine facility at Pivot Park. Built to GMP Annex 1 standards, it features advanced cleanrooms, integrated development and analytical labs, and dedicated warehousing. This investment strengthens our end-to-end support for precision medicine, meeting growing demand for high-quality, scalable nanomedicine solutions.

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End-to-End Solutions

Our Integrated Nanomedicine Platform

From program management through regulatory submission, we deliver a fully integrated nanomedicine development platform under one roof.

01

Program Management

Using the right standards at the right development phase, our comprehensive program management services streamline your nanomedicine drug development.

02

Precursor Manufacturing

Experience tailored solutions for your precursor manufacturing needs, including payloads, API, and building blocks.

03

Nanomedicine Manufacturing

Comprehensive nanomedicine development and manufacturing services from process development through GMP manufacturing.

04

Fill & Finish

State-of-the-art fill and finish capabilities ensuring seamless delivery to trial sites with clinical packaging and logistics.

05

Bioanalysis

Supporting your preclinical and clinical stages with expert nanomedicine testing services and certified bioanalytical capabilities.

06

CMC Regulatory Support

Our comprehensive CMC regulatory services streamline the preparation and submission of regulatory files for your nanomedicines.

Why Ardena

Your Partner in Nanomedicine Development

At Ardena, we offer a fully integrated approach to nanomedicine development. Our team of experts works closely with you, combining deep scientific knowledge with state-of-the-art manufacturing capabilities.

Fully Integrated Approach

A seamless workflow from payloads and building blocks through nanoparticle manufacturing, fill and finish, and bioanalysis.

Pre-clinical to Commercialization

End-to-end partnership covering every phase of development, from early research through to commercial manufacturing.

Customized Solutions

Every nanomedicine project is unique. We tailor our approach to your specific therapeutic goals and target indications.

Regulatory Expertise

Comprehensive CMC regulatory services to streamline the preparation and submission of regulatory files for your nanomedicines.

Let's collaborate

We Know Development
Let's talk about yours

Your program has a specific set of challenges. Our scientists want to hear them. Get in touch and we'll set up a direct conversation with the right expert.

Direct contact

info@ardena.com +32 9 267 65 00

Response within 1 business day

FAQ

Nanomedicine FAQ

A nanomedicine CDMO is a contract development and manufacturing organisation specialised in developing and producing nanoparticle-based medicines. Ardena is one of Europe’s most advanced nanomedicine platforms, delivering a fully integrated service , from program management through GMP manufacturing and regulatory submission – under one roof.

Ardena works across all three, so the platform is matched to your payload and delivery goal. Lipid-based systems (LNPs, liposomes, micelles, lipid nanoemulsions, solid lipid nanoparticles) suit payloads such as mRNA and oligonucleotides; polymeric nanoparticles draw on polymer synthesis and self-assembly for engineered delivery; and metal / metal-oxide nanoparticles offer customised solutions for advanced delivery and diagnostic imaging. Ardena’s team helps select the right platform for payloads including cytotoxics, oligonucleotides, mRNA, peptides and proteins.

Yes. Ardena provides comprehensive nanomedicine development and manufacturing – from process development through GMP manufacturing — for its nanoparticle platforms, including lipid nanoparticles and polymeric nanoparticles, in a purpose-built facility built to GMP Annex 1 standards. Batch sizes for Phase I and Phase II supply and 100% vial inspection.

Yes. Ardena offers tailored precursor manufacturing, including payloads, API and building blocks, as an integrated part of its nanomedicine platform.

Yes. Ardena delivers an end-to-end platform under one roof: precursor (building block) manufacturing, nanomedicine manufacturing, fill and finish, bioanalysis, and CMC regulatory support — with fill-and-finish ensuring seamless delivery to trial sites.

Yes. Liposomes are part of Ardena’s lipid-based nanoparticle platform, alongside LNPs and lipid micelles, developed and manufactured through to GMP. Advanced liposome manufacturing techniques: flow manufacture of liposomes with size control by extrusion processes.