As an RTSM partner, Veeva RTSM works with sponsors and CROs to implement our solution for new studies. Sometimes, however, we are called on to help with unique scenarios involving studies that have already begun recruitment, such as the following: The study started collecting RTSM data in a simple solution (maybe even Excel), but the …
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The Veeva Summit is a customer-focused conference where industry leaders can join to share best practices around the implementation and use of Veeva Products. This year was the Veeva RTSM team’s first Summit experience. We asked them how it went, and here is what they said about their experience: What was your impression of …
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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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Why is flexibility important to keeping a clinical trial on track? To illustrate this, let’s explore the Clinical Trial Supply Lifecycle using a fictional Sponsor named Pharzm who is running a Phase 3 trial for a new drug. Pharzm has a new two-year trial, which includes 200 subjects. They plan to manufacture 5,280 bottles of …
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An RTSM system is the tool of choice for clinical trial subject randomization and management, drug assignment, and inventory control. The RTSM system is often the first point of entry for subject data before it is pushed to the EDC housing the clinical database. So when it’s time to hold the startup meeting with your …
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