ICS Industry Differentiation
Trust us to manage your vendor relationships and optimize partnerships to ensure a smooth collaboration and drive efficiency in your clinical supply chain.
Successful Trial Execution
Maximizing Efficiency and Quality in Your Clinical Supply Chain
Our CMO/Vendor Management service provides comprehensive oversight and support to ensure seamless collaboration with your contract manufacturing organizations (CMOs) and vendors. With our expertise and attention to detail, we optimize vendor qualifications, contract negotiations, and trial design for successful trial execution.
What You Can Expect
Achieve Seamless CMO/Vendor Management
and Optimize Your Clinical Supply Chain
Enhanced Vendor Qualifications
Our expertise in conducting facility inspections and comprehensive reporting ensures that CMOs and vendors meet the necessary standards, leading to higher quality products and services.
Streamlined Contract Negotiations
Our experienced team helps optimize contract terms, including breach of contract and limitations of liability language, protecting the company and fostering mutually beneficial relationship with vendors.
Efficient Trial Design and Execution
By leveraging our knowledge in both small and large molecule trial configurations, companies can streamline their trial design, reduce complexities, and enhance the overall efficiency and success of their clinical trials.
What We Offer
Our Comprehensive CMO / Vendor Management Services
Streamlining communication, logistics, and quality control for reliable supply chain management.
Vendor Qualifications & Quality Audits
ICS can support surveillance through facility inspections of drug product and finished drug product CMO/CDMOs and contribute to final reporting
Contract Negotiations
Assistance with breach of contract and limitations of liability language to your master supply agreements
Person-in-Plant (PIP) Oversight
ICS can perform CMO/CDMO site visits to ensure proper blinding controls and ensure that high-profile jobs are Right First Time/Released On Time
Trial Design Expertise
ICS can design finished drug product / placebo control kits supporting optimal utilization in both small and large molecule trial configurations
Master & Executed Batch Record Management
ICS can edit/author Master Batch Records and ensure applicability of generic Masters for time and cost savings for sponsors
ICS can edit/author Master Batch Records and ensure applicability of generic Masters for time and cost savings for sponsors
ICS has direct experience with older and newer generation IRT/RTSM systems including natural language processing build designs