
Veeva RTSM
Streamlines subject randomization and trial supply management, ensuring timely supply availability in clinical trials.
Overview
Veeva RTSM is utilized by sponsors, CROs, and clinical sites to streamline the process of randomizing subjects and managing trial supplies. Integrated with Veeva EDC and Veeva CDB, it facilitates the transfer of patient and trial data efficiently.
With Veeva RTSM, sites can log in to conduct subject screenings, allocate randomization, assign kits, and undertake emergency unblinds swiftly when required. The system employs both basic and predictive supply algorithms to guarantee that necessary trial supplies are available precisely when needed.
One of the key features of Veeva RTSM is its modular architecture. This allows users to select and utilize only the functions they require, optimizing both costs and functionality. Flexible configuration options and customizations ensure the study design aligns with specific protocol demands, while adaptable supply settings help in controlling shipments and minimizing drug wastage.
Veeva supports the platform with proactive project management, maintaining open communication and providing expert guidance throughout the trial process, ensuring a smooth and effective site experience.
Key benefits include:
- Seamless trial execution with a focus on site experience.
- Modular solution to pay for only necessary functions.
- Flexibility in study builds with tailored customizations.
- Supply management strategies to maximize resource utilization and minimize costs.
- Comprehensive support and guidance from experienced professionals.
Consistently managed and backed by Veeva, RTSM ensures accurate and efficient randomization and supply management for a range of clinical trials.


