Clinical Research Drug Supply

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

Data Protection: PSNResearch collects, stores and processes data exclusively for the purpose of business operation and according to PSNResearch’s Data Protection Policy. Any personal information submitted to PSNResearch on the contact form is used and stored as an e-mail. PSNResearch will only store your e-mail data for as long as is necessary for the purpose of business operation. When this purpose is no longer relevant the data sets will be deleted as part of PSNResearch’s routine operations.