From import to disposal, your single source for clinical research drug supply.

Your trial is a complex, multi-phase project involving dozens or hundreds of culturally and geographically diverse stakeholders. Regulatory submission will involve clinical research data being collected, cleansed, managed, and analyzed. Patients and investigators will need to be recruited from a small population who have many choices. With all of these issues, why not leave us to manage the equally complex task of provisioning your clinical partners with the compounds involved?

We provide solutions customized to the unique and demanding constraints of your therapy. From consultancy services to identify and recommend of relevant solutions to flexible operational services, to sourcing of capacity and adding the capacity you need (supply coordinators, QP or operators) – we are the complete solution for clinical drug supply.

  • Investigational products
  • Supply management
  • Labels and label text
  • Labelling and packaging
  • Qualified person (QP), release EU, import and export
  • Storage and distribution
  • Accountability for provisioned materials, and destruction of over-supply