RTSM Resources
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Beyond the Acronyms: What Today's Trials Really Need From RTSM
12/4/2025
Consider how resin selection, process optimization, and system qualification create scalable workflows that meet evolving regulatory and operational demands in modern biomanufacturing.
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The Present And Future Of Study Supply Management
6/17/2024
Gain expert insights on the future of RTSM strategy and its evolution with the changing clinical supply and technology landscape in our webinar.
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A Custom IRT System Facilitates Precision Medicine Studies
1/29/2025
As the industry continues to embrace personalized medicine, the ability to implement and support an atypical supply chain is crucial.
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IRT. IVRS. IXRS. IWRS. RTSM
1/26/2022
The pharmaceutical industry is full of acronyms. Gain insight into the evolution of the acronyms, the technology and the terminology, specifically for RTSM (Randomization and Trial Supply Management).
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3 Study Areas Where Your IRT Vendor Should Do More
11/21/2024
Find out how advanced IRT systems now support diverse trial designs and how the expertise of RTSM vendors is crucial for tailoring solutions to trial needs and providing ongoing support.
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Blinded Randomization And Trial Supply Management Gets Support
11/17/2023
Uncover how this global specialty pharmaceutical company was able to ensure the confidentiality of its blinded study data while receiving flexible and scalable unblinded support.
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Finding The Optimal IRT/RTSM Design For Your Clinical Trial
10/4/2024
Determine the best IRT/RTSM design for your trial through consideration of the user, data collection, and future-proofing.
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Master Protocol Studies: Technology Considerations For The 'Never Ending' Clinical Trial
1/6/2022
Since the FDA is now encouraging creativity in trial designs, it is important for all stakeholders to adapt processes to follow the science and ultimately bring medicines to patients, faster. This white paper addresses the complexities that come with these trial designs, and how randomization and trial supply management (RTSM) solutions are critical to run flexible, robust, and quality-driven trials.
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5 Ways To Get Ready For IRT Regulatory Inspections
7/31/2025
Preparing for a regulatory inspection during a clinical trial can be daunting. Learn about the importance of clear roles, audit trails, data integrity, and training, and get recommendations to help.
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Human-Centered RTSM Design Enhances Data, Safety, And Operations
12/5/2025
Uncover how this human-centered approach to RTSM prioritizes user experience (UX) and interface design (UI) to reduce complexity, minimize errors, and improve compliance.