Drug Inventory Management (DIMS)
Protocol management
- Maintain oversight and manage drug schedules and dispensation for multiple protocols from a single system
Real-time visibility
- Create reports within and across your protocols for a complete view of your entire study portfolio
Control supply strategies
- Set up manual and automatic drug ordering for each site and protocol to ensure drug is where it is needed when it is needed
Comprehensive standalone inventory management
DIMS is a comprehensive solution for managing drug ordering and site inventory when the patient tracking and control of a full IRT system is not required. Simplify study team workflows and maintain oversight by automating your supply management and reporting across multiple protocols in a single sytem. Over the course of your trial, you can directly manage user access for each protocol and add protocols at any time without impacting the system or requiring additional coding.
- Supply strategy management
- Drug dispensing management
- Drug supply management
- Drug accountability and reconciliation
- Drug returns and destruction management
Flexibility allows for automated and manual drug ordering
DIMS offers the flexibility of automated and manual drug ordering set up for each of your protocols within the system. Set up automated resupply strategies to maintain appropriate inventory levels so your sites have the supply they need at all times. Our Data Transfer Module with depot integrations enables drug order requests to automatically transfer drug requests to your depots.
We know study teams need the flexibility to manage the unexpected that can frequently occur like an unexpected change in patient enrollment or on-site storage issues. So with DIMS, you can also allow manual requests to give your site teams more control in these moments without sacrificing quality. The system has built in controls allowing you to approve or reject all site requests before they go to the depot.
Maintain visibility with ad-hoc reports that you can set up for multiple protocols
Suvoda DIMS ad-hoc reports give real-time access to data points and trends with your drug inventory at the sites and depots within each protocol. Enabling you to quickly identify where supply shortages exist, redirect inventory to sites that need it most, and track drug from depot to dispensation or return and destruction. You’ll always know where your inventory stands and have the intelligence you need to make better decisions in executing on today’s trials—and planning for tomorrow’s.
Broad perspective, keen insight, and calm guidance
Seamless technology in complex trial ecosystems
Seamless technology in complex trial ecosystems
INSIGHTS & NEWS
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BLOG
Electronic Clinical Outcome Assessments (eCOA) in Clinical Trials
sept. 12, 2024 -
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4 Factors That Shape a Technical Direction That Lasts
sept. 5, 2024 -
NEWS
The cornerstone of clinical trial success: selecting seasoned CDMOs and IRT vendors
sept. 3, 2024 -
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Improving Informed Consent: A Closer Look at the Draft FDA Guidance for Patient Understanding
août 30, 2024 -
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How thoughtful adaptation in clinical trials can bring new medicines to market faster
août 15, 2024 -
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The benefits of real-time data for CROs
juil. 24, 2024 -
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Why drug pooling remains important to clinical trials
juil. 23, 2024 -
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Decoding eCOA trends: adoption predicted to rise
juil. 11, 2024 -
NEWS
Suvoda Expands its Clinical Trial Offering with the Introduction of ePatient
juin 26, 2024 -
BLOG
How CROs can meet timelines by selecting fit-for-purpose technology to run their trials
juin 26, 2024