Your trial.
Our solutions.
We have never failed to deliver to a study
Clinical trials supplied
1,000+
Suppliers and manufacturers
95+
Years of global experience
100+
Our Services
We manage the entire clinical supply chain
Case Study
Jakavi Oncology Trial
Supplying a leading CRO’s global Phase 3 study
Challenge
To supply a Phase 3 oncology trial spanning 14 countries within eight weeks and to ensure regular resupply for three years
Solution
CSI’s manufacturer relationships and depot network ensured high volumes of ruxolitinib were sourced and delivered on time
Result
Efficient supply of the product allowed scheduled Site Initiation Visits (SIVs) to take place, keeping the CRO’s study on track
Our Expertise
Six areas in which CSI excels
North America
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Canada
Guatemala
Mexico
Panama
United States
EMEA
Austria
Belgium
Bulgaria
Croatia
Czech Republic
Denmark
Egypt
Estonia
Finland
France
Germany
Greece
Hungary
Ireland
Israel
Italy
Jordan
Latvia
Lebanon
Lithuania
Netherlands
Norway
Oman
Poland
Portugal
Romania
Russia
Saudi Arabia
Serbia
Slovakia
Slovenia
South Africa
Spain
Sweden
Switzerland
Tunisia
Turkey
United Arab Emirates
United Kingdom
South America
Argentina
Brazil
Colombia
Peru
Asia Pacific
Australia
China
India
Japan
Malaysia
Philippines
Singapore
South Korea
Taiwan
Thailand
Vietnam
Global Reach
Warehouses
Offices
CSI's sourcing capabilities are served by an extensive network of audited manufacturers and suppliers, strategically positioned across 60 countries on six continents
Our Global Reach
Warehouses and offices
Our network extends to 60 countries on six continents
Our Partners
Why work with us?
Pharmaceutical and Biotechnology Companies
CSI is a proud supplier to top-ten pharmaceutical companies and leading biotechs around the world, providing tailor-made solutions and country-specific regulatory expertise to boost success rates for even the most complex global trials
Clinical Research Organisations (CROs)
Along with our smart sourcing solutions and unrivalled product access, we manage the entire supply chain, allowing CROs to concentrate on finding patients and delivering successful clinical trials – saving time, money and resources