Global Clinical Trial Supplies
Customized packaging, labeling, and distribution services
We understand the challenges of managing clinical trials at numerous sites across multiple countries. Quotient Sciences can ease the headache of global product supply logistics and accelerate your proof-of-concept timeline. We’ll develop and manufacture your drug product, then seamlessly integrate a flexible packaging, labeling, and distribution strategy that's tailored to your clinical trial.
Key questions we can help you address
- How much product do I need to manufacture?
- What packaging do I require?
- How do I ship to multiple countries?
- How do I develop a flexible supply chain?
- How often will my product be required?
- Who will coordinate the supply chain?
Getting your product to the right patient at the right time
Service benefits
- Flexible product – get the product delivered as bulk, bright stock in primary packaging, or as patient kits – the choice is yours
- Global supply – ensure distribution where it’s needed, anywhere in the world, when it’s needed
- Avoid stockpiling and product attrition at clinical sites through bright stock inventory management and just-in-time (JIT) labeling and distribution – only ship product when it’s required by a named patient
- Protect precious active pharmaceutical ingredient (API) and drug product – develop a logistics strategy that reduces waste
- Access in-depth knowledge on best practice, from local rules and regulations, through to managing import and export licensing
- Benefit from flexibility in cross protocols through drug pooling – maximize flexibility by JIT labeling to allow distribution of drug product across multiple clinical protocols
Building an effective product supply strategy is vital for rapidly moving through clinical development. Quotient Sciences has supplied over 2,000 drug products to more than 150 unique clinical sites in hospitals and contract research organizations worldwide.
Connect with us to learn how we can help support your global clinical trials.
Resources
Learn more about clinical trial supplies
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Info SheetGlobal Clinical Trial SuppliesQuotient can ease the headache of global product supply logistics and accelerate your proof-of-concept timeline. We’ll develop and manufacture your drug product, and then seamlessly integrate into a flexible packaging, labelling & distribution strategy, tailored to your clinical trial.
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Case StudiesEndevica Case Study - Peptide Program using Translational PharmaceuticsEndevica Bio is developing TCMCB07 as a novel synthetic peptide product for the potential treatment of cachexia. Read how they leveraged the Quotient Sciences Translational Pharmaceutics platform for this program.
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Case StudiesEnsysce Biosciences Case StudyRequest a copy of our latest case study with Ensysce Biosciences about how our integrated strategies helped them achieve their regulatory milestones faster for PF614-MPAR, an Extended Release product.
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Info SheetDrug-Drug Interaction (DDI) StudiesAssessing how your drug interacts with other drugs in vivo is a critical step in the drug development process and is essential in ensuring safe and efficacious drug delivery. This assessment is known as a drug-drug interaction (DDI) study and is a regulatory requirement for submissions of investigational new drugs (INDs). Learn more about Quotient Sciences' offering for DDI studies.