Global clinical supply chain management consulting services
As the only global company 100% focused on supplying your clinical trial, CSM 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. No matter how complex your clinical trial supply challenges are, our twenty-plus years of experienced supply chain management consulting allows our team to bring the expertise and background, ensuring a smooth supply process.
We treat every client as a highly valued partner of ours, guiding them through the day-to-day steps while ensuring their success at the same time, every step along the way.
Our experienced clinical trial project management team oversees your entire study from start to finish, providing exceptional, personalized customer service with a high level of flexibility and agility.
Clinical Trial Project Management Consulting
Treating every client as a partner, our team guides them through the day-to-day steps with expert clinical trial consulting. These strategic, highly competent supply chain management consultants ensure consistent successes throughout the duration of your project.
Our experienced global clinical trial project management team oversees your entire study from start to finish, providing knowledgeable and exceptional customer service as well as rapid turnaround times.
CSM 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 CSM to have the flexibility and stability to adapt our clinical trial consulting services as your study evolves.
Clinical Trial Project Management Consulting Services Include:
- IVRS/IWRS Management
- Logistics Planning
- Global Distribution and Importation
- Cold Chain
- Inventory Control
- Controlled Drug and Substance Handling
- Packaging and Labeling Operations
- Project Budgeting
- Returns, Reconciliation and Destruction
Your CSM 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 CSM provides a project manager in one of our EU sites who specifically works to globally assist and manage activities with the whole project management team.
Our agile team of project managers are 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.
Clinical Supply Chain Management Consulting Services
CSM’s supply chain management consultants 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 customizable solutions.
From customizing clinical trial study designs to applying cost-effective methods for the clinical supply chain, every step of the way we help clients plan and execute projects of all sizes and scopes.
Our customer-centric focus will make your clinical study more efficient, thereby reducing costs and improving outcomes.
CSM gives your study a clear advantage. Our highly-trained, accomplished team is empowered to provide high levels of agility and state-of-the-art clinical services. This is how we can easily accommodate any sudden changes that occur during your clinical study.
Clinical trial Supply Chain Management Consulting Services:
- Logistics Planning
- Unique Packaging Design and Labeling Solutions
- Comparator Drug and Ancillary Supplies Sourcing
- Global Studies Management (including QP release)
- Label Text Generation, Translation and Approval
- Batch Record Review and Approval
- Supply Chain Management
“I want to extend my deepest appreciation for the support and help that you have lent me on our Phase III project. Thank you for taking the time to promptly assist me with my many urgent requests. Without your help and timely guidance, I would not have been able to meet my study’s timeline.”
Sr. Clinical Data Manager, Pharmaceutical Company