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Case processing in pharmacovigilance is a fundamental activity to support safety surveillance in clinical trials. Along with an anticipated therapeutic effect, medicinal products may also carry certain risks for adverse reactions. Some of these...
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In this installment of our “Meet the Team” blog series, we talk to Jim Maciariello, General Manager of Product Design and Engineering (PD&E). We’ll...
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It should come as no surprise that conducting a clinical trial is expensive. Just how expensive depends on the phase and design of the trial, with...
9 min read
The following article illustrates how inequities arise in healthcare, one disease at a time. It highlights insights from a program we are currently...
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Our previous update1, Analysis of China’s First National Tender on Coronary Stents, discussed the first national-level centralized tender for a...
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In this installment of our “Meet the Team” blog series, we talk to Meghana Kapoor, Manager, Clinical Data Management, about her background, her...
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In this installment of our “Meet the Team” blog series, we talk to Soma Sekhar Koramatla, Associate Manager, Statistical Programming, Biometrics...
3 min read
Given the shifts that Contract Research Organizations (CROs) and the pharma industry have gone through with the COVID-19 pandemic and subsequent...
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Our previous blog discussed the emerging trends for the companion diagnostics (CDx) regulations in China. There have been several developments since...
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Many articles discussing the difference between drug and device trials come from a regulatory perspective on how clinical trials are designed and...
