Clinical trials demand care and precision. We are invested in our clients efforts of providing patient access to breakthrough treatments.

Our Belgian facility operates under strict GMP standards, but compliance alone isn't enough - we focus on getting the details right.

Complex blinding protocols require careful planning. Whether you need a solution for single-blind or intricate multi-arm crossover studies, our team handles the technical aspects while maintaining study integrity. We've safely managed packaging and labeling for protocols involving temperature-sensitive products, biologics, pediatric formulations, and controlled substances.

Packaging and Labeling for Global Clinical Trials

Multi-language labeling presents unique challenges. Global clinical trials often require at least 10-15 languages within a single booklet label. Our experts create clear, compliant layouts that satisfy regulatory requirements across different countries.

Secondary packaging goes beyond putting products in boxes. Kit assembly, randomization support, comparator and ancillary material coordination must align perfectly with study protocols. From innovators, global CRO's to Functional Service Providers, our Project Managers comfortably support and consult our clinical trial clients throughout each packaging campaign.

In-House Services Agility

In addition to having an agile production team, our single-panel and variable data printing capability enables us to quickly respond to our clients requirements. For our clients, keeping clinical label and packaging services in-house means we can offer them faster turnaround times and better quality oversight.

Our Qualified Person provides European release authority. This regulatory requirement often creates bottlenecks at larger organizations. Direct access to our QP means faster decision-making and clearer communication about release criteria.