The integrity of your pharmaceutical product doesn’t end with its formulation. The packaging and delivery systems you choose must be just as robust to preserve sterility, prevent contamination, and maintain chemical stability throughout its shelf life and distribution.

Clients face increasing pressure to select and validate packaging components that comply with global regulatory requirements. From container-closure systems to advanced delivery devices, it’s critical to understand how materials perform under stress and over time, and whether they pose risks through leachables or physical failure.

The Eurofins BioPharma Product Testing (BPT) network of laboratories provides comprehensive validation services for pharmaceutical packaging and drug delivery systems. Whether you’re working with vials, prefilled syringes, blister packs, or complex combination devices, we can help you validate your components are safe, stable, and regulatory-ready.

Our services confirm that container systems maintain a sterile barrier seal and prevent leaks or chemical interactions that could compromise product quality. These evaluations are supported by state-of-the-art instrumentation, proven methodologies, and an experienced team of scientists who understand the unique needs of biologic and pharmaceutical developers.

In addition to validation studies, we also provide clients with 24/7 access to data via our secure online portal, including shelf-life calendars and real-time project tracking. This transparency ensures you always have visibility of timelines and outcomes, helping you avoid delays and stay compliant.

Eurofins BPT works in alignment with international pharmacopeial guidelines and supports regulatory submissions around the world. Whether you’re in early development or preparing for market authorisation, we’ll help you ensure every part of your packaging and delivery system will stand up to the most stringent scrutiny.