Schedule a meeting today.
See you in Boston!
Guiding your nanomedicine candidate through its journey to the clinic
Process development, analytical development, analysis, stability testing, manufacturing
Crystal structure by X-ray, solid form screening, solid form selection, IP support
Formulation development, analytical development, manufacturing, stability studies
Packaging, labeling, clinical trial logistics
Mass spectrometry, immunochemistry, flow cytometry, in-vitro drug discovery, clinical trial services
Scientific report writing, module 3 writing, regulatory CMC support
Driving complex drug conjugates from synthesis to clinical supply
Developing and manufacturing formulations that lead to improved bioavailability
Meeting your needs from pre-clinical to small-scale commercial manufacturing
Bringing your oral drug to clinical trials quickly and reliably
Guiding you through the development of injectable drug products to GMP standards
Using the right standards at the right development phase, our comprehensive program management services streamline your small molecule drug development.
Helping you turn your compounds that show promise into GMP-grade drug substances.
We advance your clinical candidates through the pipeline quickly and safely with specialist drug product services.
Our bioanalytical platform supports your preclinical and clinical stages with expert testing services.
Our comprehensive CMC regulatory services streamline preparation and submission of your registration file.
Using the right standards at the right development phase, our comprehensive program management services streamline your large molecule drug development.
We advance your large molecule candidates through the pipeline quickly and safely with specialist drug product services.
Our bioanalytical platform supports your large molecule drugs through preclinical and clinical stages with expert testing services.
Our comprehensive CMC regulatory services streamline the preparation and submission of the regulatory files for your large molecule drug.
Using the right standards at the right development phase, our comprehensive program management services streamline your nanomedicine drug development.
We turn your nanomedicine candidates into suitable drugs with specialist development and manufacturing services.
Our bioanalytical platform supports your preclinical and clinical stages with expert testing services.
Our comprehensive CMC regulatory services streamline the preparation and submission of the regulatory files for your nanomedicines.
Agile and reliable, we guide you and your molecule through the complexities of drug development.
A legacy of scientific excellence, development expertise and integrated solutions.
Seven GMP/GLP facilities across Europe and the US, supporting innovation.
Driving responsible growth through sustainable practices, ethical governance, and respect for people.
Defining who we are and how we work together to achieve excellence with purpose and care.
Guided by experienced industry leaders, our Board ensures strategic direction and excellence.
An international and diverse team of scientific and industry experts driving our progress and success.
A dynamic, passionate, and growing team with opportunities to learn and make an impact.
Join Ardena at the 15th American Drug Delivery & Formulation Summit (DDF Summit) 2025, taking place September 15–16 at The Westin Copley Place in Boston, Massachusetts, USA.
This premier event brings together over 300 scientific leaders from pharma, biotech, and drug delivery industries to discuss innovative solutions to the greatest challenges in pharmaceuticals, biologics, and device development.
Meet our delegates:
Aditya Kulkarni, PhD – Director, Business Development
Chrissa Schremp – Director, Business Development
Don’t miss the presentation by:
Hibreniguss Terefe, PhD – Director, Research and Development, with his talk “Blueprint for Bioavailability: A Scalable Formulation Roadmap for Challenging APIs.”
Visit us at our booth #4 to connect with our experts.
Our team is eager to discuss how Ardena’s integrated services can accelerate your drug development programs from formulation and bioanalysis to manufacturing and regulatory support.
Schedule a meeting today.
See you in Boston!