Study Setup Centre
Building a strong reputation in life sciences and healthcare takes time, consistent delivery, and proven compliance across temperature-controlled logistics, chain of custody, and audit-ready documentation.
Over 25 years, CRYOPDP has earned credibility through consistent delivery of reliable, compliant, temperature-controlled logistics solutions for life sciences and healthcare.
The Study Setup Centre provides tailored services to support investigators in meeting the compliance and documentation requirements of critical studies. We focus on reliability, specialist expertise, and a controlled experience that investigators can trust.
With CRYOPDP as your Study Setup Centre, you receive the shipment details required for each consignment, including documentation, chain of custody requirements, and defined temperature requirements:
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Comprehensive Starter Pack
The study initiation pack includes essential documentation, templates, and start-up materials.
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Study Logistics Information
Call-in and pickup cut-off times were kept up to date to support accurate scheduling and coordination.
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Investigator Manual
Protocol-aligned instructions that guide shipment handling, documentation, and procedures.
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Local Supply of IATA Compliant Packaging and Air Waybills
We provide IATA-compliant packaging and air waybills from in-country stock. We include supporting documentation. This enables compliant shipping and smoother processing.
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Range of Packaging Options
We offer controlled ambient, refrigerated, frozen, and cryogenic packaging. Each option is selected to match the temperature profile, lane requirements, and study needs.
Dedicated Study Set-Up Centre for Clinical Trial Supply Shipments
Bringing new medicines to market requires controlled planning, regulatory alignment, and disciplined execution. From Phase I to Phase IV, clinical trials need 24/7 operational oversight and temperature-controlled logistics across global supply chains.
We plan each study early in development and build tailored delivery programmes for temperature-controlled logistics, based on the product profile, temperature range, lane requirements, and regulatory expectations. Each programme aligns with recognised cold chain and distribution standards, including those published by the European Medicines Agency, to minimise risk, support customs coordination, and maintain full regulatory compliance across international clinical supply chains.
Our goal is to support clinical trial success through controlled execution, full traceability, and consistent temperature-controlled logistics, from study start-up through delivery.