Eurofins’ new Clinical Trial Supplies makes the complex simple

Sandra Hageman, Senior Director Marketing, Eurofins BioPharma Services, Clinical Trial Testing and Supplies, Sandra.Hageman@bcl.eurofins.com

As a new business unit within the Eurofins network of companies, the Clinical Trial Supplies purpose-built cGMP facility in Horsham, PA, US, offers primary and secondary packaging, labelling, QP services and global distribution of Investigational Medicinal Products (IMP), as well as Advanced Therapy Medicinal Products (ATMP) in support of phase I to phase IV clinical trials. The opportunities and synergies this facility will bring to BioPharma clients is profound.

Built from a blank canvas by a team of industry veterans, the operations, processes, and IT systems were designed to offer exceptional service levels with fast turnaround times, beating the current industry standards: On-demand Packaging and Just-in-Time Packaging. By deploying a global Enterprise Resource Planning (ERP) solution from day one, these new services are “Agile by Design” with a superior quality mindset to begin helping patients globally.

Further capabilities include labelling services, getting the right drug to the right patient, taking into account randomisation and blinding in complex and adaptive clinical trial protocols, decentralised clinical trials support (direct to patient), comparator sourcing and schedule I-V, and controlled substance storage services.

A clinical trial cannot run without the drug on time – patients are always our focus

This remarkable addition to the Eurofins network of companies marks a significant step forward in our commitment to excellence and innovation. This facility is more than just an addition; it is an expansion of our global footprint and collaboration with the Eurofins CDMO network of companies, and a testament to our dedication to delivering quality clinical trial solutions efficiently and consistently. For more information, visit: https://eurofinscentrallaboratory.com/clinical-trial-supplies/