Multi-Regional Clinical Trials: Key Recommendations for a Global Clinical Development Program
The FDA recently released a draft guidance on the use of multi-regional clinical trials (MRCTs) in oncology research.
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Veristat Blog : Published
AI is changing clinical development, but speed alone isn't enough. In a regulated industry, every output still has to be accurate, traceable, and ready to withstand regulatory scrutiny.
That's the central theme of Veristat’s Kyle McBride's recent conversation on the Life Sciences Today podcast with Healthcare IT Today.
Kyle discusses why successful AI adoption in biostatistics depends on more than large language models or automation. It requires validated systems, expert oversight, and workflows built specifically for clinical development.
Listen to the full episode if you're interested in the future of AI in clinical research.
The Discussion Covers:
The FDA recently released a draft guidance on the use of multi-regional clinical trials (MRCTs) in oncology research.
Clinical trial leaders in small and medium-sized biotech companies regularly find themselves at the intersection of growing requirements, shrinking...
FDA guidance and EMA regulations are frequently updated to govern the planning, conduct, and reporting of clinical trials for drug development. Stay...