Clinical supply chain management
Clinigen is committed to working closely with you and your team to better plan, prepare, and manage your study. Many challenges can occur when planning the set-up and design of a study. Our 25+ years of experience in supply chain management allows our team to bring the expertise and background needed to ensure a smooth supply process, no matter how complex your clinical trial supply challenges are.
Managing your Clinical Supply Chain project
We treat every client as a highly valued partner of ours, guiding them through the day-to-day steps while ensuring their success along the way. Our highly competent supply chain management consultants ensure consistent results throughout the duration of your project.
We oversee your entire study from start to finish, providing knowledgeable and exceptional customer service as well as rapid turnaround times.
Clinigen is focused exclusively on clinical trials and brings a high level of expertise to every supply chain management consulting project, ensuring we apply the best methods and practices to your specific clinical study.
Our client-focused management approach allows us to quickly adapt our services as your study evolves.
Clinical Trial Supply Chain Management Services Include:
- IVRS/IWRS Management
- Logistics Planning
- Global Distribution and Importation
- Cold Chain
- Comparator Drug and Ancillary Supplies Sourcing
- Inventory Control
- Controlled Drug and Substance Handling
- Global Studies Management (including QP release)
- Unique Packaging and Labelling Solutions & Operations
- Label Text Generation, Translation, and Approval
- Project Budgeting
- Returns, Reconciliation and Destruction
- Batch Record Review and Approval
Your Clinigen team also includes a backup clinical support services project manager who can seamlessly take control of your project if the lead clinical trial project manager is unavailable.
Furthermore, for global clinical trials, Clinigen provides a project manager in one of our EU sites which specifically works to assist and manage activities globally with the whole project management team.
Our agile team of project managers is available at any time for updates or inquires and can ensure that they are up to date and familiar with all aspects of the clinical trial.
Risk-based optimisation
Having a flexible supply strategy is critical for running an effective clinical trial. Our partner N-SIDE’s proprietary software suite, leveraging advanced optimisation algorithms and forecasting techniques coupled with cutting-edge analytics, enables greater efficiencies for your trial, including waste reduction, proactive risk management, and accelerated timelines.
Risk-based optimisation of clinical trial supplies allows for proactive as well as reactive risk management. Through technology, we can provide an accurate picture of a global clinical trial supplies project and its integrated parts in real-time. This enables informed decisions regarding drug allocation and reduces inefficiencies at every step of the way. These clinical trial simulations facilitate the daily management of a study, advise on ideal drug overage to use, and allow quick reaction in case of outliers, thus securing trial continuity.
Clinical supply chain management consulting services
Clinigen’s supply chain management experts spend the time necessary to get to know every client, ensuring every step in the clinical supply chain meets their precise needs in order to create tailored solutions.
From customising clinical trial study designs to applying cost-effective methods for the clinical supply chain, we help clients plan and execute projects of all sizes and scopes.
Our customer-centric focus will help make your clinical study more efficient, thereby reducing costs and improving outcomes.
Clinigen gives your study a clear advantage. With flexibility at our very core, we can easily accommodate any sudden changes that occur during your clinical study.