Trial Wisely

Partner Network

Close relationships with specialist tech firms and full-service CROs are fueling our innovative IRT, eConsent, and eCOA solutions
Collaboration

We think we’re all wiser when we work together. So we collaborate not just within Suvoda, but across the industry as well.

We partner with organizations across every touchpoint of a clinical trial so that your studies can move faster and easier than ever. In our rapidly-evolving industry, collaboration bridges the gaps between technologies to eliminate digital silos and improve efficiency across the entire clinical trial continuum.
Collaboration

We think we’re all wiser when we work together. So we collaborate not just within Suvoda, but across the industry as well.

We partner with organizations across every touchpoint of a clinical trial so that your studies can move faster and easier than ever. In our rapidly-evolving industry, collaboration bridges the gaps between technologies to eliminate digital silos and improve efficiency across the entire clinical trial continuum.

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. 

FORECASTING
n-side

Learn more →

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.  

Learn more about our partnership

View partner site


Temperature excursion
berlinger-logo

Learn more →

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.

Learn more about our partnership

View partner site →


Electronic Data Capture (EDC)
Veeva_Logo

Learn more →

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

Learn more about our partnership

Cytel-Logo-png-format     PSI     syneos

     

     

WCT_company-logo       Inno logo_tagline_20 Years_EN[3]     Treximo Logo transparent

 

This integration created simplicity at every level, removed manual data entry, and brought cohesiveness to all the stakeholders involved in our program.”
Catherine Munera, Ph.D., Cara Therapeutics

Partner with us

Let’s build more empowering experiences for sponsors, sites, and patients, together. Just fill out the form below to get started.