Captivate®. Accelerating Clinical Trials®

⎯⎯⎯  Captivate RTSM

#00D5FF#7C3AED#CD19B2#00D5FF#7C3AED
Randomization and Trial Supply Management

Randomization and Trial Supply Management system

#380669#A855F7#EC4899#380669#A855F7
RTSM Built for
Modern Interventional Studies
Configure randomization, preserve blinding, and manage trial supplies seamlessly within the Captivate clinical data platform.

Robust Randomization Strategies

Captivate RTSM is a web-based Randomization and Trial Supply Management module designed to support a wide range of randomization strategies while maintaining operational simplicity, compliance, and audit readiness.

Efficient Trial Supply Management

Built for sponsors and CROs running interventional studies, Captivate RTSM delivers robust randomization capabilities without the overhead and rigidity of traditional IRT systems.

Unified Clinical Data Environment

Designed to integrate seamlessly with the Captivate clinical data platform, Captivate RTSM enables study teams to configure and manage randomization schemes, maintain blinding, and track investigational kits within a single, unified environment.

#380669#A855F7#EC4899#380669#A855F7
Robust Randomization
Design electronic informed consent materials that reflect your protocol, study population, and regulatory requirements. Customizable presentation of consent materials for complex requirements.
1

Simple Randomization

Easily configure simple randomization logic for straightforward study designs.

2

Stratified Randomization

Support for randomization across protocol-defined factors to ensure balance.

3

Permuted Block

Configurable block sizes for permuted block randomization strategies.

4

Dynamic Randomization

Support for dynamic randomization to maintain balance across treatment arms in real-time.

5

Real-Time Enforcement

Enforcement of randomization rules at the point of assignment for compliance.

6

Centralized Management

Logic managed centrally for consistent application across all sites and subjects.

#22D3EE#A855F7#EC4899#22D3EE#A855F7
Blinding and Unblinding Controls
Built-in support for blinded study designs while preserving participant safety and regulatory compliance. Rules are enforced at the system level to prevent unauthorized access.

Single & Double Blind

Comprehensive support for both single- and double-blinded designs

Role-Based Access

Protects blind integrity through controlled access levels

Emergency Workflows

Controlled and logged emergency unblinding workflows

Complete Audit Trails

Full traceability for all unblinding events during the study

#380669#A855F7#EC4899#380669#A855F7
Integrated Kit
Identification and Tracking
Pair randomization with structured kit ID setup and tracking to support investigational product oversight. Centralized configuration for subjects and sites.
1

Centralized Setup

Define kit identifiers centrally for efficient oversight across the study.

2

Automated Assignment

Assignment of kits based directly on randomization results.

3

Lifecycle Tracking

Complete tracking of kit status throughout the entire study lifecycle.

4

Supply Visibility

Visibility into used, assigned, and available kits for sites and study teams.

#380669#A855F7#EC4899#380669#A855F7
Streamlined Workflows
Intuitive, role-driven workflows designed to minimize training and operational friction for sites and central teams.

Secure Browser Access

Secure, web-based interaction with the RTSM module

Guided Assignments

Step-by-step workflows for randomization and kit assignment

Immediate Confirmation

Real-time confirmation for all randomization actions

Subject History

Clear visibility into individual subject and kit history

C   S Weight Lift scaled
#22D3EE#A855F7#EC4899#22D3EE#A855F7
Integrated With
The Captivate Platform
Operate within the broader Captivate ecosystem for consistent configuration and unified oversight.

Shared Context

Shared subject and study context with Captivate EDC.

Unified Audit Trails

Consistent tracking across randomization, kits, and clinical data.

Simplified Reporting

Exports and reports that include critical randomization metadata.

Reduced Effort

Minimized reconciliation effort across clinical systems.

#380669#A855F7#EC4899#380669#A855F7
Security, Compliance And Control
Designed to meet global regulatory expectations and support audits throughout the study lifecycle.

Compliance with 21 CFR Part 11 and Annex 11

Secure system access and data handling

Comprehensive audit trails for randomization and blinding

Documented traceability for inspections and monitoring

#380669#A855F7#EC4899#380669#A855F7
Integrated Kit
Identification and Tracking
Pair randomization with structured kit ID setup and tracking to support investigational product oversight. Centralized configuration for subjects and sites.
1

More Flexible

Avoids the rigidity of systems that require extensive customization.

Platform_Core
2

More Structured

Highly auditable alternative to manual or spreadsheet-based randomization.

Platform_Core
3

No Extra Overhead

Designed to support study needs without unnecessary operational burden.

Platform_Core
#22D3EE#A855F7#EC4899#22D3EE#A855F7
Who Uses Captivate RTSM
Used by sponsors and CROs running interventional clinical trials that require reliable randomization and controlled blinding.
Phase I–III Clinical Trials
Stratified Studies
Blinded Trials
Trials seeking Integrated Randomization
#380669#A855F7#EC4899#380669#A855F7
Why Study Teams
Choose Captivate
1

Robust Support

For multiple randomization methods

2

Blinding Controls

Built-in support for unblinding

3

Integrated Kit Tracking

Aligned with randomization outcomes

4

Unified Workflows

Consistent context with Captivate EDC

5

Inspection-Ready

Auditability without unnecessary complexity

Ready to Learn More?

Discover how Captivate can support your clinical research needs. Our team is here to answer questions and show you what’s possible.

Scroll to Top