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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Though this is the first year since Veeva acquired Veracity Logic to form Veeva RTSM, the team and system have a 16-year history of successfully partnering with sponsors and CRO’s, helping them simplify subject management, randomization, and trial supply. The system is fast, intuitive, and complete – its modular and highly configurable design system allows …
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You may have heard about how easy it is to navigate the Veeva RTSM system. To illustrate this, we’ve added an overview demo video to our resources page. This video guides a site user through the key pages of the system. This video guides a site user through the key pages of the system. In …
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I’ve just attended my first in-person Veeva EU Summit event. It was inspiring to see the energy, enthusiasm, and passion from the Veeva customers and my colleagues in Zurich. Jim Reilly, VP of Development, Veeva Cloud Strategy, introduced Veeva RTSM to the audience during the opening keynote session. That kicked off the incredible flurry of …
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Despite your team’s careful planning, unexpected road bumps can occur when a clinical trial is in the field. We hope none of these happen to you, but here’s how a nimble RTSM would help you handle these situations. Someone left the package out in the heat! Problem: Your drug must always remain within a …
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Drug accountability is important to gathering quality data as well as ensuring patient safety. The problems associated with it remain key issues for clinical trial management in 2022. Using an RTSM (IRT/IVR/IWR) system to manage the distribution and assignment of an investigational product (IP) is a well-established practice. Most RTSM systems include some method of …
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The Challenge: As technology becomes more and more sophisticated, data collection systems for clinical trials are at risk of becoming less intuitive for users. The challenge for the pharma-tech industry is obvious: how to deliver more power while remaining user-friendly for the diverse population of users at clinical sites around the world. The Solution: …
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The Clinical Trials industry has seen its share of changes over the past 20 years (like many industries). In case you are keeping score, or trying to keep score, this blog should clarify things a bit. IVR or IVRS (Interactive Voice Response System) is a tool used in the 1990s/early 2000s to call into a …
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