Clinical Trial Drug Supply –
Unrivalled access to the commercial medicines needed to run clinical trials
Our expert team is committed to providing you with reliable, sustainable, and ethical access to the comparator drugs you need for your clinical trial, ensuring supply continuity for the duration of the study.
We personalise supply strategies to provide you with unrivalled access to commercial medicines (comparator drugs, standard of care, co-meds, adjuvant therapies) and ancillaries, as well as direct access to a global network of manufacturers and approved distributors.
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Let us guide you through the complexities of the clinical supply process. Speak with our team of experts today.
Let's talkGlobal reach.
Local expertise.
Local expertise.
Through our global manufacturer and authorised distributor partnerships we provide access to commercial medicines from all the key markets around the world. Whether you need bulk supply of commercial drug from a central location or locally sourced product to be shipped direct-to-site, we have the global reach combined with the local insight and expertise to come up with the optimum drug supply solution for your clinical trial.
Central Supply
Through our network of direct manufacturer partnerships we can facilitate large bulk orders of commercial drugs needed for clinical trials, ensuring you have them manufactured to your exact specification and suppled with all associated documentation.
Demand driven supply
We provide access to regular volumes of comparator drugs on a more frequent basis, with associated documents, enabling sponsors to adapt the supply forecast to the real-time study demand, ultimately reducing waste and cost.
Local Sourcing
Our local supply solution provides access to the commercial medicines you need within the country they are to be used. Through our network of local authorised distributors we remove the need for complex and costly import processes by locally sourcing the commercial medicines and supplying them directly to the site in-country.
Going beyond drug supply
When supplying comparator drugs into global clinical trials, simply supplying the product is not enough. Our experienced team work with you to translate the study protocol and country list into an optimal supply plan which goes beyond the product supply, ensuring that you have access to the documentation needed and processes in place to allow for seamless supply to clinical trial sites around the world.
Bespoke Supply Strategies
Reviewing the study design and country list to create an optimal supply plan.
Dedicated Project Management
Assigned to your account for global study support.
Adaptive Approach
Providing a flexible solutions to ensure cost effectiveness and supply sustainability.
Waste Reduction
On-demand and local sourcing options to adapt to the evolving needs of your study.
Kick off and regular review meetings
A focus on continuous improvement and developing long-term trusted partnerships.
Committed to Quality
The right people and technologies to ensure the highest quality outputs.
Trusted manufacturer partnerships
Through our trusted manufacturer relationships, we can provide the associated documentation required to allow the products to be used across all study countries, including:
Certificate of Analysis (CoA)
TSE/BSE Statements
Batch Release Certificates
Certificate of Conformance (CoC)
Stability Data Reports
Equivalency Statements
Manufacturer Safety Data Sheets
Equivalency Statements
First Leg
Documentation
