SmartSignals RTSM

Randomization & Trial Supply Management

Streamlined randomization meets optimized supply management 

Make your supplies go further

  • Reduce overage requirements
    Direct medication only to where the study needs it, limiting wastage and reducing overage needs, using our proprietary algorithms.
  • Optimize medication expiry
    Ship and dispense medication to optimize shelf life.
  • Understand ongoing study supply needs
    Plan mid-study production based on accurate study usage data.
  • Save medication across study programs
    Pool supplies across studies to further optimize medication supply requirements.

How does RTSM improve efficiency?

SmartSignals Randomization and Trial Supply Management (RTSM) addresses the logistical complexities inherent in patient randomization and investigational product management by streamlining and condensing processes.

1

Design

Configurable checklists allow you to skip duplicative design calls and source document reviews, and you can visualize your system during configuration.

2

Implementation

Deploy your RTSM system in 1-4 weeks after kickoff using Signant’s agile, iterative design process that handles even the most complex randomization schemes and dosing schedules.

3

Management

Handle mid-study changes with ease using the same optimized design process, and lean on support from a dedicated project team and 24/7 helpdesk from system build to study close.

Retire your spreadsheets or
slow, costly IVR/IWR systems

SmartSignals RTSM effectively manages randomization and optimizes the trial supply chain to reduce waste and guarantee that the right patients get the right products at the right time. We are ready to support your traditional, virtual, or hybrid trials with a direct-to-patient model of clinical supply delivery and management to give you the visibility and control regardless of protocol design, randomization schemes, or other complex requirements.

Why choose SmartSignals?

SmartSignals RTSM is a trusted and foundational component to any study, relied on by top sponsors and CROs as the only platform that offers a single source for: 

  • Rapid deployment
    Signant’s streamlined design/build approach allows us to fully implement RTSM twice as fast – one to four weeks compared to eight weeks or more with other solutions, and this same process is applied to protocol amendments to quickly accommodate mid-study changes.
  • Integration
    RTSM seamlessly blends with Signant’s end-to-end evidence generation and clinical trial management solutions including eCOA and clinical supplies management as well as with third parties for electronic data capture and manufacturing solutions.
  • Clinical and operational support
    Not technology for technology’s sake, Signant’s RTSM solution provides the mobile apps, user-focused features, and product support you expect as well as guidance from our clinical science, biostatistical, project management, and business intelligence experts who shepherd your RTSM deployment from inception to system archival.

Leverage Signant’s experience

With Signant’s RTSM, you leverage over 20 years of experience implementing more than 2000 protocols in 90 countries. Count on Signant’s full-service RTSM to lay the operational groundwork your study needs to effectively generate evidence.   

Frequently Asked Questions

What is RTSM in clinical trials?

RTSM stands for randomization and trial supply management. It refers to a technology solution used in clinical trials to control patient randomization and manage drug dispensation.

What is the purpose of randomization in clinical trials?

Randomization is a method of experimental control that prevents selection or accidental bias. Randomization forms the basis for statistical tests.

What is clinical trial supply management?

Clinical trial supply management is typically a computer-controlled system used in clinical trials to dispense and manage site inventories.

Can Randomization & Trial System Management be accessed on a mobile device?

With Signant’s SmartSignals RTSM solution, mobile applications are available through both Apple and Google stores. If your study is set up for mobile access, you may log in with the same credentials you used on the web.

Can I use Signant’s Randomization & Trial System Management system to unbind a subject?

For double blind trials, our RTSM solution enables a function for authorized users to unblind a patient in an emergency. The user manual and/or study monitor can provide additional guidance.

How do I fix a data entry error in the system?

The DCF may be found on the landing page upon login, or please contact the Helpdesk for additional support.

Want to learn more?

Discover how RTSM and other building blocks in our end-to-end SmartSignals suite optimize clinical trials to help you produce accurate evidence.