The world's most innovative
Randomization and Trial
Supply Management

Prancer
The world’s first 100% configurable Randomization and Trial Supply Management Solution

Your RTSM should adapt as trials evolve, without disruption. The complexity of today’s trials is inadequately supported by traditional RTSM solutions, typically requiring custom coding to deliver system changes – costing you both time and resources. As trial complexity continues to increase, shouldn’t your system keep up?

Prancer brings both speed and flexibility to clinical trials, enabling your trial to ebb and flow as needs change, all while offering exceptional quality and performance.

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Prancer RTSM Differentiators

Speed

Rapid study start-up with Natural Language Processing (NLP)

Combined with our modern technology stack, NLP technology enables Prancer to read and interpret written RTSM specifications, understand them, and build a deployable system automatically.

speed
revolutionized study build

Revolutionized Study Build

Approve the System, not 200+ pages of complex specifications

Our iterative build process allows us to refine the system prior to UAT due to increased transparency and customer involvement. Therefore, UAT becomes a final check, not a process to find bugs in the software.

Robust Forecasting

Solve complex clinical supply forecasting challenges

Our integrated and intuitive forecasting engine enables visibility, impact assessment and control over supply decisions.

robust forecasting
Post go-live flexibility

100%

configurable and flexible

Post Go-Live Flexibility

Follow the path of science without disruption

Our 100% configurable and flexible RTSM enables faster system changes from 1 hour (simple) up to 2 weeks (complex). Since flexibility is built in, you can shift gears mid-study to follow the science. Your RTSM will never hold you back.

Unparalleled Functionality

Cohort Management
  • Flexibility to adjust cohorts based on results
  • Control over screening caps and enrollment
  • Reduce supply overage and waste
  • Full transparency into protocol amendments and cohort versions

Unparalleled Functionality

Returns, Accountability & Destruction
  • Ensure single source for performing reconciliation at the end of a study
  • Report kit status throughout the study
  • Enable CRO oversight and workflow management
  • Manage accountability needs based on study, all the way to controlled substances

Unparalleled Functionality

ISTs/IITs
  • Avoid wasted supply
  • Ensure transparency of IST status
  • Ability to pool supply across all ISTs in that program
  • Support sunshine reporting with shipment records

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What is Agile RTSM, Really?

Not all RTSMs that reference being agile are based on the software methodology. The difference may impact your study.

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Unparalleled Functionality

Clinical Supply Pooling
  • Share inventory across multiple studies to conserve your supplies: at a lot level as well as at a site level
  • End user ability to adjust which studies have access to which lots
  • Resupply forecasting calculates demand across all sites that can use the inventory, regardless of study

Unparalleled Functionality

Temperature Excursion Tracking
  • Track excursions of shipments to sites as well as on-site excursions
  • Upload or enter excursion details, defined per study
  • Exhaustive options for defining statuses of the kits affected

4G Clinical

RTSM Best Practices

RTSM Technology has Evolved to Let the Science Lead

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Seeing is believing. Let us show you first-hand how Prancer enables faster, more flexible and higher quality systems.

 

 

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Start a conversation today. Our data sheet provides a snapshot of Prancer RTSM's differentiators and exceptional services.

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Featured Resources

Modern Technologies in Clinical Trials

Modern Technologies

Demystifying the use of Innovative RTSMs in a Highly-Regulated Environment

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Disrupting Study Start-Up

Faster Study Start-Up

How Natural Language Processing (NLP) is a Game Changer in Clinical Research

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Disrupting Study Start-Up

Disrupting Study Start-Up

How Agile RTSM Software Development Accelerates the Clinical Trial Timeline

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