August 20th, 2025 WRITTEN BY Fresh Gravity
Clinical trials are advancing, but outdated design processes continue to place a heavy, often unmeasured burden on patients. This whitepaper introduces a patient-centric, quantitative approach to modelling burden that can improve both ethics and efficiency in trials. Read more in the full whitepaper.
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Written by Neha Sharma, Sr. Manager, Data Management In today’s data-driven landscape, governance without transparency is like navigation without a map. As organizations strive to strike a balance between agility and control, Transparent Policy Centers are emerging as a powerful framework to unify data policies, enforce governance, and empower business users simultaneously. But what does […]
Written by Colin Wood, Strategy & Solutions Leader, Life Sciences Regulated drug development is inherently document-centric, requiring a vast array of structured documents to support regulatory submissions and maintain licenses. With the rise of Generative AI tools like ChatGPT, Copilot, Gemini, and Claude, organizations now have unprecedented capabilities to process, summarize, and generate documentation. At […]
Written By Preeti Desai, Sr. Manager, Client Success and Colin Wood, Strategy & Solutions Leader, Life Sciences In the previous blog, we established that we can no longer afford to treat CMC data as something created just for submissions. This data holds immense operational and strategic value for analytics, process optimization, and automated regulatory submissions. But to unlock that value, data quality and structure are paramount. We also […]
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