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Precision in Trial Randomization
Randomization and Trial Supply Management
Efficiently manage randomization and trial supply logistics with ResearchManager RTSM. Streamline processes, reduce risks, and ensure accurate, real-time tracking to support your clinical trials, all while maintaining compliance and reducing costs.
✔ Real-time tracking & visibility
✔ Streamlined randomization & supply management
✔ Fully compliant with regulatory standards
25%
Reduction in randomization setup time
Speeds up the setup process for randomization procedures.
30%
Faster randomization
Reduces the time needed for participant randomization.
40%
Improved shipment tracking efficiency
Enhances shipment tracking, leading to faster and more accurate insights.
Validated Randomization
Thanks to validated forms of randomization, results from clinical research are reliable. We are talking about regular randomization, site-specific randomization, and randomization with random blocks. These diverse options and flexibility empower research teams to choose the most suitable method for their study. With RTSM, study owners quickly gain insight into the reliability and completeness of their research without unnecessary time and resource expenditure. A must-have for clinical research involving patient participation.
Optimal Inventory Management
RTSM enables precise tracking of shipments, preventing excess and shortages. Moreover, RTSM flexibly adapts to changing needs within clinical research, minimizing waste and optimizing inventory management. This results in cost savings and a smooth flow of the research process.
Real-time Insight
ResearchManager RTSM provides real-time insight into inventory chains and randomization processes of ongoing and completed research, with comprehensive audit trails for regulatory compliance. RTSM is the tool for optimal and accurate management of inventory usage and precise monitoring, resulting in an efficient flow of the research process.
Highlighted features
Dynamic Randomization Methods
Perform a variety of randomization techniques, including stratified and blocked randomization, to ensure balanced and unbiased assignment of participants to treatment groups.
Stratification
Enhance randomization by incorporating stratification to account for specific participant characteristics. This approach improves the accuracy and reliability of study outcomes.
Blinding and Unblinding Capabilities
Maintain study integrity with robust blinding procedures, while allowing for secure and controlled unblinding when necessary.
Real-Time Inventory Tracking
Monitor drug supply levels in real-time across all sites, ensuring timely replenishment and minimizing the risk of stockouts.
Shipment Tracking
Track the status and location of study drug shipments, ensuring timely delivery and minimizing delays in participant treatment.
Notifications
Receive notifications for events such as participant randomization, stock replenishment, and low inventory levels.
Audit Trail
Complete audit trail functionality to document all modifications to the data, including the user who made the change, the timestamp of the change, and a detailed description of the alteration.
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Discover why ResearchManager drives clinical trial success.
All-in-one suite for every stage of clinical research
The Clinical Research Suite (CRS) is an all-in-one solution for managing Clinical Data and Operations, from trial planning to completion. CRS provides a cost-effective solution by combining multiple tools and services into one platform, reducing the need for multiple vendors.
Scalable Solutions for Organizations of All Sizes
The Clinical Research Suite scales to meet the needs of any organization. Small organizations can choose the Pay-as-you-go On Demand model, while mid-size and large organizations benefit from the Enterprise package with structured plans for multiple ongoing studies, ensuring efficient resource management and growth.
Fast-go live within 5 working days
The Clinical Research Suite (CRS) offers a fast go-live option within 5 working days. Additionally, fully customized implementations are available, tailored to specific needs, ensuring the platform aligns perfectly with trial requirements.
Dedicated team with personalized support
Experienced in-house second-line assistance and a dedicated account manager are always included to ensure seamless operations and personalized guidance throughout the entire process.
Proven success
With over 20,000 studies conducted, 8,000+ active users, and more than 1,000,000 patients enrolled, ResearchManager’s Clinical Research Suite (CRS) has a proven track record of delivering successful clinical trials worldwide.
Compliance and Technical Information
ResearchManager is compliant
- Offices in the Netherlands (HQ) and in the USA.
- ISO 27001 certified
- NEN 7510 certified
- ISO 14155 compliant
- 21 CFR PART 11 compliant
- GCP compliant
- GDPR compliant
- HIPAA compliant
- Secure connection with Comodo’s EV SSL certificate
Data Centers and Cloud Services
1) Data Centers in the EU
- TIER 3+
- SOC 2 security standards
- ISO 9001 certified
- ISO 14155 certified
- ISO 27001 certified
- NEN 7510 certified
- Dedicated backup server, AES 256 encrypted
2) Regional Cloud Services
ResearchManager provides localized cloud services in various regions (e.g., USA, Canada, Australia, UK, Japan), ensuring compliance with regional data residency regulations. This guarantees that data is stored and processed within the respective country’s jurisdiction, adhering to local security and compliance standards.
Thierry Wetting
International Sales Manager
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