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Global trial logistics specialists

The globalisation of clinical trials requires country-specific regulatory expertise. Pharmaceutical and biotech companies must be able to understand changes around international drug sourcing and import and export requirements to remain compliant. With global experience spanning six continents, CSI provides targeted solutions to serve trials worldwide, sourcing and supplying medicines, medical devices and ancillaries to Europe, the United States, Central and South America, and Asia-Pacific.

Pharmaceutical and Biotechnology Companies

It has been very beneficial working with the CSI team. They have excellent scientific expertise, clearly understood the challenge, and provided outstanding solutions. Their global reach allowed us to tap into many markets. They are customer-focused, result-driven, and we enjoyed working with them. Well done, Team!
Director of Drug Product, Formulation  & Stability
at a leading gene therapy Biotechnology company

The gold standard for the clinical trial supply

Pharmaceutical and biotechnology companies are increasingly facing pressure to move candidates through the clinical trial pipeline quickly. Greater need for efficiency requires an expert comparator sourcing and supply chain partner that can alleviate disruptions to timelines, costs and product availability. CSI helps to grow trial pipelines and optimise trial performance. We are a proud supplier to top-ten pharmaceutical companies and leading biotechs.

Reducing risk, boosting success

CSI reduces risk across every part of the supply chain, boosting trial success rates by ensuring delivery of the right comparator drugs, devices and services at the right place and time, even for the most complex adaptive clinical trials.

Managing the entire supply chain

CSI manages the entire supply chain, allowing CROs to concentrate on finding patients and delivering successful trials. Our seamless supply management operations and distribution solutions ensure CROs can operate efficiently, saving time, money and resources.

Clinical Research Organisations (CROs)

Six areas of expertise drive CSI’s ability to effectively source comparators, medical devices and ancillaries:

  • Protocol interpretation
  • Product access
  • Supply continuity
  • Cost control
  • Speed
  • Supporting documents

​​A truly global footprint

Our CRO partners conduct studies all over the world. CSI’s strong global presence and expertise means we can support even the most complex studies and clinical supply requirements. With warehouses in more than 50 countries, we can efficiently and consistently provide solutions across Europe, the United States, Central and South America, and Asia-Pacific.

The science of clinical trial supply

CSI provides secure and transparent sourcing of products for a broad range of clinical trials across all therapeutic indications. With decades of combined experience in drug development, our team provides fully integrated, one-stop solutions. We pride ourselves on our ability to assist our partners with comparator identification, strategic guidance around the protocol, and cross-market regulatory advice.

Expertise you can rely on

Clinical trial supply chains require robust planning and management to ensure successful, reliable delivery. We provide regular forecasts to optimise timelines, ensure quality, maintain safety, comply with security standards, and remain on budget.

Quality is in our DNA

With longstanding relationships with MHRA and EMA, CSI’s regulatory and quality assurance experts provide expert advice. All our teams stay up to date with the latest government and agency requirements around the world, while our country-specific regulatory expertise minimises risk and guarantees compliance.

Adding value from the outset

By partnering with hospitals and research centres at an early stage of their studies, CSI can comprehensively assess clinical trial requirements from the outset, providing strategic solutions and utilising our extensive sourcing expertise. As a dedicated sourcing solution provider, CSI streamlines the entire procurement process, allowing researchers and healthcare professionals to focus on their core activities.

Hospitals and Academic Institutions

We take on the extra burden

We supply a diverse range of medications, comedications, ancillary products – such as lab kits, clinical site files and test tubes – and provide a printing service. This relieves our partners of administrative burdens, allowing them to focus their resources on trial patient recruitment.

Handling every aspect of trial supply

While Clinical Research Associates (CRAs) handle site qualification, CSI takes charge of assessing the study protocol and providing the necessary trial support services:

  • Calculating product quantities

  • Negotiating competitive pricing
  • Coordinating delivery schedules
  • Managing inventory levels
  • Minimising supply shortages and wastage

Your partner for cutting-edge research

CSI works closely with world-class academic institutions, universities, hospitals and research centres that are producing cutting-edge medical research. We support their clinical trials by providing a wide range of cost-effective and compliant comparator medicines and ancillaries.

A history of working together

CSI’s Managing Director, Vanessa Dekou, is on the advisory board of Chelsea and Westminster Hospital in London and the Judge Business School at the University of Cambridge. CSI also has a history of close collaboration with University College London, providing internship and career opportunities following Vanessa’s own studies there.

The trusted global partner of leading pharmaceutical and biotechnology companies, Clinical Research Organisations (CROs), hospitals and academic institutions

Our partners work tirelessly to improve patient outcomes and quality of life. At CSI we accelerate drug development by designing and delivering highly efficient and robust supply chains that allow our partners to deliver their clinical trials on time and budget.

Get in touch with a member of our experienced team today to discuss your clinical trial supply requirements

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