Clinical Supplies Management
From label generation and global coordination to specialized packaging and SOP authoring, our comprehensive services ensure efficient trial execution and regulatory compliance.
Clinical Supplies Management
Enhance Trial Efficiency With Professional Clinical Supplies Management
Our expertise and in-house programmatic software handle complex trial designs, label generation and translation, global distribution coordination, specialized packaging, sourcing of comparator drugs, inventory controls, and SOP authoring. With meticulous attention to detail, we streamline logistics, ensure regulatory compliance, and optimize inventory control.
What You Can Expect
Seamless Coordination and Control of Clinical Trial Supplies
Trust us to manage your clinical supplies with professionalism and precision.
Enhanced Efficiency
Experience improved efficiency in managing clinical supplies, resulting in streamlined operations, reduced delays, and optimized trial timelines.
Cost Savings
Benefit from effective inventory control, optimized packaging, and labeling solutions, minimizing waste and reducing unnecessary expenses.
Regulatory Compliance
Achieve regulatory compliance in clinical supplies management, ensuring accurate labeling, proper documentation, and adherence to regulatory guidelines, leading to successful regulatory inspections and approvals.
What We Offer
Our Comprehensive Clinical Supplies Management Solutions
Streamlining your clinical trial supplies for success
Complex Clinical Trial Designs (Phase I-IV, Compassionate Use, EAP)
ICS uses in-house programmatic software designed specifically for clinical trials ranging from 50-30,000 patients
Label Text Generation, Translation, & Approval
ICS can create Master English and assist with regulatory review, translation certification services and approval in Label Management Services software
Coordination of Global Distribution & Importation
ICS can coordinate with your CDMO depot management to ensure import licenses/permits and pro-forma invoicing is correct
Specialized Packaging & Labeling Solutions
ICS can review your clinical protocols and stability plans to ensure proper packaging design and component lead times are in place allowing packaging/labeling campaigns execute on schedule
Sourcing of Comparator Drugs/NIMPs & Ancillary Supplies
ICS can help align country participation and filing requirements with CoA and Pedigree purchasing
Packaging Design & Configuration Solutions
ICS can recommend packaging designs that meet your study needs and offer convenience and compliance for study participants
Inventory Controls, Study Drug Returns, Reconciliation & Destruction
ICS places an equal emphasis on the reverse supply chain to support study close-out and TMF readiness
Coordinate Expectations for QP Management
ICS can manage QP run, move and queue times by notating which documents are needed for review ahead of job pack release
SOP Authoring for CMC & Supply Chain Processes
ICS can author and provide editorial support for various GMP run-the-business requirements like Label Approval, Bulk and Finished Drug Destruction, Temperature Excursions and Blinding needs