About us
Company profile
We are a CDMO focused on filling, finishing, and lyophilizing injectable (bio) pharmaceutical products. We operate from our EMA and US-FDA-approved production site in Oss, the Netherlands. We can support the entire drug life cycle; from producing materials for toxicology studies to clinical material manufacturing (Phase I-III) as well as efficient preparation for PPQ campaigns and final market production using two automated filling lines. We also provide specialized small-scale (hand fill) services for personalized medicines, ensuring precision and flexibility.
We have the means, the motivation & expertise and infrastructure to bring your invention from the lab bench to the clinic and to the market. We are an experienced and reliable partner and we believe that every client is unique and important and therefore deserves personalized attention through tailor-made solutions. What sets us apart is our commitment to collaboration and flexibility throughout the process, all within the framework of the EMA and US-FDA rules and regulations.
In addition, we offer a broad range of support services such as process and formulation development, lyo-cycle development and/ or optimization, analytical development & validation, technical transfer, scale-up, process validation, stability studies, label & pack (including serialization), and final batch certification for release to clinic or market.
Ultimately, BioConnection drives healthcare innovation through strategic collaborations and emerging trend partnerships. While we do not engage in pharmacovigilance, our drug products are manufactured to meet strict quality standards that support this crucial aspect of the drug life cycle. We are committed to global health initiatives and sustainable manufacturing practices, improving access to life-saving medicines worldwide. Therefore, we would be delighted to discuss how we can support your projects.


Our mission
Being your partner of choice in the (Bio)Pharmaceutical industry
BioConnection fulfills the needs of innovative and generic (bio)pharmaceutical companies by offering flexible state-of-the-art development and GMP-compliant manufacturing services for sterile Drug Products, both commercial and clinical.
Being your partner
of choice in the
(Bio)Pharmaceutical industry
How we work

We have the means and expertise to bring your invention from the lab bench to the clinic and to the market. Utulizing our European network of development and manufacturing partners, we are able to provide tailor-made solutions and unchallenged flexibility.
At BioConnection, we believe that every client is unique, and every project deserves personalized attention and a tailor-made solution. We have a team of experienced and dedicated people across the (bio)pharmaceutical life cycle to ensure this.
A dedicated point of contact from our Program Management team will coordinate your project, together our specialists from the Quality and Production departments, we will enable you to get the best possible results.
What sets us apart is our commitment to collaboration and flexibility throughout the process all within the framework of the EMA and US-FDA rules and regulations.
Meet our team










Let's connect
If you’re exploring fill & finish support for an upcoming or ongoing program, we’d love to learn more about your goals and how we can contribute to your success. Whether you’re evaluating partners for a new project or preparing for your next development milestone, our team is ready to support you with clarity, expertise, and flexibility.
Share a few details about your molecule, timelines, or specific challenges, and we’ll follow up with insights tailored to your needs. By understanding your priorities early, we can determine how our capabilities, capacity, and approach align with your plans. We’re here to help.










