At Suvoda, we partner with other best-in-class technology companies who share our philosophy of practical innovation to solve real problems for sponsors, CROs, sites, and patients. Through close collaboration between our respective services and product teams, coordinated product roadmaps, and standardized integrations, we bring a consultative approach to address the specific challenges and needs for each sponsor or CRO. Leveraging these relationships, sponsors and CROs are able to expedite trial start up timelines, enable studies to run more smoothly, and reduce study team burden.
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Reduce cost, time and carbon footprint in your clinical supply process with N-SIDE's forecasting, simulations and optimizations. Suvoda’s real-time integration with N-SIDE's Supply App allows sponsors and CROs to optimize site and depot resupply based on actual study data. Users can make real-time adjustments to study supply parameters in Suvoda IRT, based on N-SIDE's machine learning analysis.
Reduce Drug Waste and Optimize Supply Chain
Avoid patient drop-out due to supply storage at sites while minimizing the amount of drug manufactured and distributed to depots and sites.
Reduce Cost and Timelines
Accelerate study timelines by avoiding patient dropout due to lack of drug supply at site. Avoid costly change orders for adjustment of IRT supply parameters.
Increase Study Team Efficiencies
Save study teams’ time on data integration, avoid inefficiencies and reduce human error associated with complex manual analysis. Real-time data transfer between Suvoda IRT and N-SIDE's forecasting systems increases quality and study teams’ efficiencies.
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Turn your temperature excursion data evaluation into a same-day automated process with a standard API-integration between Berlinger’s temperature data loggers and Suvoda IRT. The streamlined integration of Suvoda IRT with Berlinger’s Q-Tag data loggers enables your study team to:
Improve Efficiency
Automatically identify and quarantine impacted study kits instead of manually assessing temperature excursions.
Increase Confidence
Real-time tracking and recording of temperature controlled shipments offers greater confidence in treatment safety and efficacy.
Decrease Drug Waste
Immediate alerts of temperature deviations trigger Suvoda IRT to automatically quarantine individual drug units. This allows your site to rapidly assess and release or destroy, reducing safety risk.
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Experience simplicity, mitigate risk, and improve efficiency in your patient’s data journey. Our partnership with Veeva provides a seamless API-integration of Suvoda IRT with Veeva Vault CDMS, so that your study team can have:
- Reliable: A field-tested, streamlined integration led by experienced integrations and product teams
- Improved efficiency: Predefined, standard specifications to expedite new study configurations
- Mitigated risk: Reduced manual data entry and associated need for reconciliation
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