At Cure Pharma, we don't just offer services—we deliver tailored solutions that help clinical teams manage complexity, reduce risk, and maintain control across every stage of the clinical supply chain. Whether you need comprehensive project oversight or support with a specific challenge, we provide end-to-end coordination with full compliance and transparency.
Clinical Supply Management
End-to-End Coordination. Single Point of Contact.
From planning to last-mile delivery, we manage your supply chain so you can focus on your trial.
Clinical supply is more than logistics—it's a critical enabler of your trial timeline and data integrity. Cure Pharma manages sourcing, transport, storage, QP release, and packaging as an integrated process.
What You Gain:
- Single point of contact for all supply components
- Aligned timelines and proactive risk management
- Flexible setup, from full-service to modular
- GDP/GMP-compliant vendor network
Comparator Sourcing
Fast, Compliant Access to the Medicines Your Trial Needs
Timely sourcing of originators, generics, and biosimilars through a global network.
We work directly with manufacturers and licensed distributors to source comparator and reference products efficiently and with full documentation. Our sourcing is designed to support timelines, reduce risk, and maintain regulatory integrity across markets.
What You Gain:
- Access to originator, generic, and biosimilar products
- Batch-specific sourcing
- Full documentation (CoA, CoC, etc.)
- Coordination with depot, QP, and distribution
Labelling & Repackaging
Clinical Kits That Match Protocol and Country Requirements
GMP-compliant packaging and labelling solutions designed for global trials.
From relabelling market packs to building custom kits, our packaging services meet the unique demands of clinical trials. We support blinding, multilingual labelling, and tamper-evident packaging—ensuring your product is delivered ready for patient use, wherever required.
What You Gain:
- GMP-grade primary and secondary packaging
- Country- and protocol-specific labelling
- Blinding, randomization, and kit assembly
- Integrated release and delivery
QP Release & Regulatory
Release Without Delays. Compliance Without Uncertainty.
QP services and regulatory alignment that keep your supply chain moving.
Our Qualified Person (QP) release services meet EU GMP requirements and integrate seamlessly with logistics, documentation, and vendor oversight. We help ensure timely batch certification, documentation review, and import coordination—so compliance is never a bottleneck.
What You Gain:
- Full QP release for EU clinical trials
- Documentation review (IMPD, CoA, etc.)
- Import readiness and batch tracking
- Harmonized with storage and sourcing
Let's Build a Smarter Clinical Supply Chain Together
Whether you need a turnkey solution or support with a specific part of your supply chain, Cure Pharma is built to adapt. Let's make clinical supply simpler, faster, and more reliable—together.