Clinical Trial Supply Solution

At PRESBIO, we offer end-to-end solutions for the supply and management of clinical trial medicines and support materials across global research sites. With deep expertise in regulatory compliance, global sourcing, and time-critical logistics, we ensure seamless delivery of investigational and comparator drugs for Phase I–IV clinical trials.

We proudly support CROs, pharma companies, and research institutions by ensuring trial supplies are available on time, in spec, and in compliance — regardless of geography or complexity.

Why Partner With Us?

Expertise in multi-country clinical trial supply coordination
Fast turnaround for urgent trial supply needs and protocol amendments
Access to a wide network of authorized global suppliers
Proven track record in supporting trials across oncology, infectious disease, neurology, immunology, and more

Trial Types We Support

Phase I to Phase IV Clinical Trials
Bioequivalence Studies & Pharmacokinetic Studies
Investigator-Initiated Trials (IITs)
Compassionate Use / Expanded Access Programs

What We Offer

As part of our Clinical Trial Supplies vertical, our services include:

Global Sourcing of Comparator & Reference Drugs We procure branded, generic, and orphan drugs from authorized and GMP-certified manufacturers for use in clinical trials, including hard-to-source molecules.
Cold Chain & Temperature-Controlled Logistics End-to-end GDP-compliant logistics for temperature-sensitive products with real-time monitoring, including -20°C and -80°C shipments.
Supply Chain Management & Forecasting Inventory planning, batch tracking, and re-supply coordination to prevent stockouts or overages throughout the clinical trial lifecycle.
Regulatory & Documentation Support Expert guidance and full documentation for import/export, product qualification, and trial-related regulatory filings.

Global Reach

We manage clinical trial supply chains across Asia, Europe, North America, the Middle East, and Africa, with robust processes to handle customs, clearances, and import license requirements.