In this video interview, James Cheong, senior vice president of Asia Pacific at Precision for Medicine, outlines why faster recruitment, local data requirements for registration, and lower costs make APAC attractive for global Phase III programs.
|Articles|July 20, 2017
TrialScope Adds Seven Additional Languages to Trial Results Summaries Portal
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Patient-centric clinical trial transparency and compliance solutions company, TrialScope, announced that the Trial Results Summaries Portal now supports trial summaries in English and seven additional languages-Chinese, French, German, Japanese, Polish, Russian, and Spanish.
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In today’s ACT Brief, we examine how China’s trial startup timelines compare with those in the US and Europe, whether AI-drafted clinical study reports speed drug development, and how Bimzelx compared with Skyrizi in psoriatic arthritis.
AI can draft a CSR in minutes, but the report only reflects evidence that has already converged, so faster drafting shifts the bottleneck to upstream reconciliation, database-lock readiness, and human accountability rather than shortening the trial itself.
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In today’s ACT Brief, we examine why outdated views of Asia Pacific trial sites persist, how community access gaps reflect both patient costs and site infrastructure, and how VeonGen has aligned with the FDA on a pivotal gene therapy trial design.
Risk-based quality management depends on knowing what to monitor and on interpreting what the signals mean.
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