Highly rated by customers | 4.2 / 5 stars

Randomization Trial Supply Management Software

ResearchManager RTSM provides software for reliable randomization and accurate inventory management within clinical research, with real-time visibility and full traceability throughout the research process.

Up to 25% faster design of randomization
Up to 30% faster randomization during the study
Up to 40% more efficient inventory and distribution management

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Fully compliant with relevant laws and regulations

One RTSM solution for randomization and inventory management.

Reliable randomization and controlled medication administration are essential in clinical research. Yet many teams still work with manual or fragmented systems, leading to errors and delays. ResearchManager RTSM unites randomization, inventory management and monitoring in a single solution, with real-time control and full traceability throughout the study.

Validated randomization for reliable study results

ResearchManager RTSM supports several randomization methods, including standard randomization, randomization by site and block randomization. All methods are fully validated and conform to applicable guidelines.

Inventory and distribution management

With ResearchManager RTSM, inventories and shipments are accurately tracked and managed. The system prevents shortages and surpluses and adapts flexibly to changing study needs. Thus, waste and costs are reduced and delays are avoided.

Key Features

Controlled randomization and allocation

Support for block randomization and stratification
Randomization by site and by patient
Fully configurable by protocol
Test environment for validation of randomization schemes

Medication and inventory management

Real-time visibility into inventory levels by site
Full tracking of shipments and distribution
Automatic alerts for shortages or surpluses
Records of issuance, returns and destruction
Batch and lot number management with full traceability

Compliance, security & integrations

Role-based access rights
Support for Single Sign-On (SSO).
Two-factor authentication
Validated electronic signatures
Full audit trail of all actions
Compliant with FDA 21 CFR Part 11 and ICH-GCP
Secure data storage in compliance with ISO 27001, GDPR and HIPAA
Import and export capabilities in various formats
REST API for reading and writing data

Trusted by 200+ organizations

For more than 13 years, CROs, sponsors, universities and healthcare organizations have relied on Clinical Research Suite every day for structured and reliable clinical research. Find out how we help organizations conduct studies more efficiently, compliantly and with complete control.

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