Empower Your Clinical Supply Chain Journey From Start to Finish.
What are the biggest challenges you currently face in clinical supply chain management? Do your clinical supply strategies fulfill your trial’s Site Initiation Visits (SIV) and resupply needs? At Clinical Supply Consulting (CSC), we guide you through every step of the supply chain process—helping you keep your clinical trials and programs on track.
Streamline Study Start-Up—Avoid Delays and Save Costs.
Have you ever delayed a SIV or missed a patient dose due to a lack of a supplies? With the cost of clinical trial delays at approximately $600,000 (and potentially as high as $8 million) per day1, the importance of the right forecast cannot be ignored. Our experts help you:
- Interpret and optimize supply strategies
- Forecast supply needs to maximize availability, use-by date, and cost savings
- Identify and manage the best vendors based on your clinical program and trial
IRT Experts That Keep Your Study on Track.
Who has time to navigate through extensive system requirement documents? Let CSC take the lead in simplifying your IRT management process. Trust us to partner with your internal departments and subject matter experts (SMEs) to meticulously vet, implement, and manage your IRT to fit your study-specific needs, including:
- Oversight of the IRT study build process
- User Acceptance Testing (UAT) for the selected IRT solution
- Ongoing support for supply activities throughout the clinical trial lifecycle
- Real-time analysis with recommendations for system enhancements to optimize efficiencies
Optimize Your Clinical Trial Supplies with Efficiency in Study Conduct.
At CSC, we work closely with your Clinical Operations team to develop and manage a clinical forecast that enables us to optimize inventory management, shipping, transfer costs, and dispensing fees. We manage your clinical research needs throughout your trial and program lifecycle, with:
- Timely distribution and resupply of investigational supplies
- Temperature excursion management
and reporting - Budget and vendor management, analysis, and more
Manage Your Study Close-Out with Certainty.
As your clinical trial ends and sites prepare for closure, trust us to orchestrate the close-out activities with efficiency, certainty, and GCP compliance.
- Ensure seamless drug return, destruction at depot, and reconciliation
- Close-out all third-party vendor services and contracts with budget reconciliation
- Documentation consolidation for your Electronic Trial Master File (eTMF)
Discover What We Can Do for You.
Looking to connect with one of our experts? From study launch to close-out, we are available whenever you need us, every step of the way. Let’s get started today!