Veeva RTSM enables sponsors to dynamically add dose levels and cohorts in the user interface. This dynamic functionality allows sponsors to quickly adapt their study design based on the most recent trial data and results. https://rtsm.veeva.com/wp-content/uploads/2025/02/Creating-a-Cohort-and-a-Dose-Level.mp4 If you have questions or would like additional information on how Veeva RTSM can be your enterprise standard, then …
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By: Vincent Puglia, RTSM Strategy | Community Director Introduction: Onboarding is vital for the smooth conduct of clinical trials in today’s dynamic environment. In a recent Veeva RTSM webinar, we explored the details of an onboarding model that demonstrates excellent sponsor oversight. This method simplifies the onboarding process and enables all stakeholders to perform well …
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Introduction A main goal of Phase 1 trials is to establish the recommended dose and/or dosing regimen of new drugs for efficacy testing in Phase 2 trials, using a detailed and monitored dose escalation process. To reach this endpoint, study designs will have many components of this process outlined in the protocol, including starting dose/regimen, …
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Introduction As Sponsors look to leverage technology in clinical trials to help maintain and control adherence to the design, methodology and all aspects of a protocol, they are often left with only two functionality options to control protocol deviations. They can leverage Soft Stop functionality where a warning message is shown, providing information that may …
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Veeva’s Clinical Database can centrally aggregate, clean, and transform data from multiple sources. Learn more about how this works by clicking on the video below. If you have questions or would like additional information on how Veeva RTSM and Vault EDC can offer connectivity without compromising functionality, please reach out to your Veeva Account Partner …
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I recently attended the Clinical Trial Supply Europe conference with my colleagues Romain Arnaud, Glen Fisher, and Jennifer England. It was wonderful to connect with both familiar and new faces on a whole host of clinical supply topics. The team had so many thoughts and ideas coming out of this that it was difficult to …
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Watch how RTSM enables Supply Management through IP Release.
Regardless of the resupply strategy you adopt, designated users are also able to request manual shipments in Veeva RTSM if needed. This video will explain how.
This video provides a high-level overview of Batch Handling within Veeva RTSM, which includes both blinded and unblinded batches and determines details such as the expiration date of kits.