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Our own Tracy Mayne recently sat down with Web Sun to talk about the current state of clinical trials on the pharmaphorum podcast. One of the biggest potential paradigm shifts on the horizon is the elimination of placebo groups in some trials in favor of synthetic controls drawn from historic data. While this shift in methodology should allow more patients access to life-saving treatments, the devil is in the details. Implementing this kind of trial, getting the right data, and getting regulators to sign off are all serious challenges. Expect to learn: 👉 What exactly is meant by "real-world data" 👉 Where the data lives and what its quality is 👉 How the data can be made to function in a clinical trial 👉 Common hurdles in getting the FDA to accept conclusions 👉 Practical steps to create robust data while protecting patient privacy Listen here: https://lnkd.in/dyNqkx9Q

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Tom Natal

Partner at Slipstream IT

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Take a minute to get Tracy's perspective on the future of Clinical Trials!

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